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

Medicine

Producción científica: Contribución a una revista › Comentario/debate › revisión exhaustiva

19 Citas (Scopus)

Resumen

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.

Idioma original	English
Páginas (desde-hasta)	521
Número de páginas	1
Publicación	American Journal of Human Genetics
Volumen	99
N.º	2
DOI	https://doi.org/10.1016/j.ajhg.2016.07.015
Estado	Published - ago. 4 2016

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Publisher Copyright:
© 2016 American Society of Human Genetics

ASJC Scopus Subject Areas

Genetics
Genetics(clinical)

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Journal Article
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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

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.
En: American Journal of Human Genetics, Vol. 99, N.º 2, 04.08.2016, p. 521.

Producción científica: Contribución a una revista › Comentario/debate › revisión exhaustiva

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, n.º 2, pp. 521. https://doi.org/10.1016/j.ajhg.2016.07.015

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 ago. 4;99(2):521. doi: 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)). En: American Journal of Human Genetics. 2016 ; Vol. 99, N.º 2. pp. 521.

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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.}",

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AU - Tuschl, Karin

AU - Clayton, Peter T.

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AU - Gulab, Shamshad

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AU - Singhi, Pratibha

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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.

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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.

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