A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases

Title
A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases
Authors
Keywords
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Journal
JOURNAL OF INVESTIGATIVE DERMATOLOGY
Volume 135, Issue 11, Pages 2876-2879
Publisher
Elsevier BV
Online
2015-06-17
DOI
10.1038/jid.2015.227

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