Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018))

Karin Tuschl; Peter T. Clayton; Sidney M. Gospe; Shamshad Gulab; Shahnaz Ibrahim; Pratibha Singhi; Roosy Aulakh; Reinaldo T. Ribeiro; Orlando G. Barsottini; Maha S. Zaki; Maria Luz Del Rosario; Sarah Dyack; Victoria Price; Andrea Rideout; Kevin Gordon; Ron A. Wevers; W. K.‘‘Kling’’ Chong; Philippa B. Mills

doi:10.1016/j.ajhg.2016.07.015

Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018))

Karin Tuschl
, Peter T. Clayton
, Sidney M. Gospe
, Shamshad Gulab
, Shahnaz Ibrahim
, Pratibha Singhi
, Roosy Aulakh
, Reinaldo T. Ribeiro
, Orlando G. Barsottini
, Maha S. Zaki
, Maria Luz Del Rosario
, Sarah Dyack
, Victoria Price
, Andrea Rideout
, Kevin Gordon
, Ron A. Wevers
, W. K.‘‘Kling’’ Chong
, Philippa B. Mills

Department of Paediatrics and Child Health, Division of Woman and Child Health, Medical College, Pakistan

Research output: Contribution to journal › Comment/debate

20 Citations (Scopus)

Abstract

The American Journal of Human Genetics 90, 457–466; March 9, 2012) In this article, Figure 1 contained an error regarding the position of the deletion detected in the affected individuals of family A. The no-call SNPs between the coordinates 218,057,426 and 218,158,564 (GRCh36) suggest that exons 3 and 4 of SLC30A10 are deleted, whereas the original figure showed that exons 1 and 2 were deleted. The corrected Figure 1 and its legend are shown here. The authors regret the error.

Original language	English (US)
Pages (from-to)	521
Number of pages	1
Journal	American Journal of Human Genetics
Volume	99
Issue number	2
DOIs	https://doi.org/10.1016/j.ajhg.2016.07.015
Publication status	Published - 4 Aug 2016

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Tuschl, K., Clayton, P. T., Gospe, S. M., Gulab, S., Ibrahim, S., Singhi, P., Aulakh, R., Ribeiro, R. T., Barsottini, O. G., Zaki, M. S., Del Rosario, M. L., Dyack, S., Price, V., Rideout, A., Gordon, K., Wevers, R. A., Chong, W. K. K., & Mills, P. B. (2016). Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018)). American Journal of Human Genetics, 99(2), 521. https://doi.org/10.1016/j.ajhg.2016.07.015

Tuschl, Karin ; Clayton, Peter T. ; Gospe, Sidney M. et al. / Erratum : Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018)). In: American Journal of Human Genetics. 2016 ; Vol. 99, No. 2. pp. 521.

@article{cc9c0b707f034cc2aab41954375c7d96,

title = "Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018))",

abstract = "The American Journal of Human Genetics 90, 457–466; March 9, 2012) In this article, Figure 1 contained an error regarding the position of the deletion detected in the affected individuals of family A. The no-call SNPs between the coordinates 218,057,426 and 218,158,564 (GRCh36) suggest that exons 3 and 4 of SLC30A10 are deleted, whereas the original figure showed that exons 1 and 2 were deleted. The corrected Figure 1 and its legend are shown here. The authors regret the error.",

author = "Karin Tuschl and Clayton, \{Peter T.\} and Gospe, \{Sidney M.\} and Shamshad Gulab and Shahnaz Ibrahim and Pratibha Singhi and Roosy Aulakh and Ribeiro, \{Reinaldo T.\} and Barsottini, \{Orlando G.\} and Zaki, \{Maha S.\} and \{Del Rosario\}, \{Maria Luz\} and Sarah Dyack and Victoria Price and Andrea Rideout and Kevin Gordon and Wevers, \{Ron A.\} and Chong, \{W. K.{\textquoteleft}{\textquoteleft}Kling{\textquoteright}{\textquoteright}\} and Mills, \{Philippa B.\}",

note = "Publisher Copyright: {\textcopyright} 2016 American Society of Human Genetics",

year = "2016",

month = aug,

day = "4",

doi = "10.1016/j.ajhg.2016.07.015",

language = "English (US)",

volume = "99",

pages = "521",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

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number = "2",

}

Tuschl, K, Clayton, PT, Gospe, SM, Gulab, S, Ibrahim, S, Singhi, P, Aulakh, R, Ribeiro, RT, Barsottini, OG, Zaki, MS, Del Rosario, ML, Dyack, S, Price, V, Rideout, A, Gordon, K, Wevers, RA, Chong, WKK & Mills, PB 2016, 'Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018))', American Journal of Human Genetics, vol. 99, no. 2, pp. 521. https://doi.org/10.1016/j.ajhg.2016.07.015

Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018)). / Tuschl, Karin; Clayton, Peter T.; Gospe, Sidney M. et al.
In: American Journal of Human Genetics, Vol. 99, No. 2, 04.08.2016, p. 521.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018))

AU - Tuschl, Karin

AU - Clayton, Peter T.

AU - Gospe, Sidney M.

AU - Gulab, Shamshad

AU - Ibrahim, Shahnaz

AU - Singhi, Pratibha

AU - Aulakh, Roosy

AU - Ribeiro, Reinaldo T.

AU - Barsottini, Orlando G.

AU - Zaki, Maha S.

AU - Del Rosario, Maria Luz

AU - Dyack, Sarah

AU - Price, Victoria

AU - Rideout, Andrea

AU - Gordon, Kevin

AU - Wevers, Ron A.

AU - Chong, W. K.‘‘Kling’’

AU - Mills, Philippa B.

PY - 2016/8/4

Y1 - 2016/8/4

N2 - The American Journal of Human Genetics 90, 457–466; March 9, 2012) In this article, Figure 1 contained an error regarding the position of the deletion detected in the affected individuals of family A. The no-call SNPs between the coordinates 218,057,426 and 218,158,564 (GRCh36) suggest that exons 3 and 4 of SLC30A10 are deleted, whereas the original figure showed that exons 1 and 2 were deleted. The corrected Figure 1 and its legend are shown here. The authors regret the error.

AB - The American Journal of Human Genetics 90, 457–466; March 9, 2012) In this article, Figure 1 contained an error regarding the position of the deletion detected in the affected individuals of family A. The no-call SNPs between the coordinates 218,057,426 and 218,158,564 (GRCh36) suggest that exons 3 and 4 of SLC30A10 are deleted, whereas the original figure showed that exons 1 and 2 were deleted. The corrected Figure 1 and its legend are shown here. The authors regret the error.

UR - https://www.scopus.com/pages/publications/84994141748

U2 - 10.1016/j.ajhg.2016.07.015

DO - 10.1016/j.ajhg.2016.07.015

M3 - Comment/debate

AN - SCOPUS:84994141748

SN - 0002-9297

VL - 99

SP - 521

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 2

ER -

Tuschl K, Clayton PT, Gospe SM, Gulab S, Ibrahim S, Singhi P et al. Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018)). American Journal of Human Genetics. 2016 Aug 4;99(2):521. doi: 10.1016/j.ajhg.2016.07.015

Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018))

Abstract

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