A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases.
作者信息
Chmel Nadja, Danescu Sorina, Gruler Amelie, Kiritsi Dimitra, Bruckner-Tuderman Leena, Kreuter Alexander, Kohlhase Jürgen, Has Cristina
机构信息
Department of Dermatology, Medical Center-University of Freiburg, Freiburg, Germany.
Department of Dermatology, University "Iuliu Hatieganu", Cluj-Napoca, Romania.
出版信息
J Invest Dermatol. 2015 Nov;135(11):2876-2879. doi: 10.1038/jid.2015.227. Epub 2015 Jun 17.
PMID:26083552
Abstract
摘要
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