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Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant.
Genetics in Medicine ( IF 8.8 ) Pub Date : 2020-09-15 , DOI: 10.1038/s41436-020-00969-y
Eliane Beauregard-Lacroix 1 , Guillermo Pacheco-Cuellar 1 , Norbert F Ajeawung 2 , Jessica Tardif 1 , Klaus Dieterich 3 , Tabib Dabir 4 , Dina Vind-Kezunovic 5 , Susan M White 6 , Denes Zadori 7 , Claudia Castiglioni 8 , Lisbeth Tranebjærg 9, 10 , Pernille Mathiesen Tørring 11 , Ed Blair 12 , Marzena Wisniewska 13 , Maria Vittoria Camurri 1 , Yolande van Bever 14 , Sirinart Molidperee 2 , Juliet Taylor 15 , Alexandre Dionne-Laporte 16 , Sanjay M Sisodiya 17, 18 , Raoul C M Hennekam 19 , Philippe M Campeau 1
Affiliation  

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

中文翻译:

更正:DOORS 综合征和复发性截断 ATP6V1B2 变体。

本文的修订版已发布,可通过本文顶部的链接访问。
更新日期:2020-09-15
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