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.
N1 - Publisher Copyright:
© 2016 American Society of Human Genetics
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.
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U2 - 10.1016/j.ajhg.2016.07.015
DO - 10.1016/j.ajhg.2016.07.015
M3 - Comment/debate
C2 - 27486784
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 -