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

Résultat de recherche: Comment/debateexamen par les pairs

19 Citations (Scopus)

Résumé

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.

Langue d'origineEnglish
Pages (de-à)521
Nombre de pages1
JournalAmerican Journal of Human Genetics
Volume99
Numéro de publication2
DOI
Statut de publicationPublished - août 4 2016

Note bibliographique

Publisher Copyright:
© 2016 American Society of Human Genetics

ASJC Scopus Subject Areas

  • Genetics
  • Genetics(clinical)

PubMed: MeSH publication types

  • Journal Article
  • Published Erratum

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