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

JOURNAL OF INVESTIGATIVE DERMATOLOGY (2015)

Journal

JOURNAL OF INVESTIGATIVE DERMATOLOGY

Volume 135, Issue 11, Pages 2876-2879

Publisher

NATURE PUBLISHING GROUP

DOI: 10.1038/jid.2015.227

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Categories

Dermatology

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