DOCK6突变导致与脑和眼异常相关的一种独特的常染色体隐性亚当斯-奥利弗综合征变体。

DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies.

作者信息

Sukalo Maja, Tilsen Felix, Kayserili Hülya, Müller Dietmar, Tüysüz Beyhan, Ruddy Deborah M, Wakeling Emma, Ørstavik Karen Helene, Bramswig Nuria C, Snape Katie M, Trembath Richard, De Smedt Maryse, van der Aa Nathalie, Skalej Martin, Mundlos Stefan, Wuyts Wim, Southgate Laura, Zenker Martin

机构信息

Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.

Medical Genetics Department, Istanbul Medical Faculty, Istanbul, Turkey.

出版信息

Hum Mutat. 2015 Nov;36(11):1112. doi: 10.1002/humu.22830. Epub 2015 Aug 7.

DOI:10.1002/humu.22830

PMID:26457590

Abstract

The original article to which this Erratum refers was published in Human Mutation 36(6):593–598(DOI:10.1002/humu22795).The authors realized that a co-author, Nuria C. Bramswig, was left off of the title page of this article at the time of submission. This erratum serves to correct this error by including Dr. Bramswig and Dr. Bramswig's institution in the title page information.The authors regret the error.

摘要

本勘误所涉及的原文发表于《人类突变》第36卷第6期，第593 - 598页（DOI: 10.1002/humu22795）。作者意识到，在提交本文时，共同作者努丽娅·C·布拉姆斯维格未被列入文章标题页。本勘误旨在通过在标题页信息中加入布拉姆斯维格博士及其所在机构来纠正这一错误。作者对该错误表示遗憾。