Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome.

Annals of Dermatology 2016;28(4):503-505

doi:10.5021/ad.2016.28.4.503

Seung Joon OH ¹ ; Song Ee KIM ; Sang Eun LEE ; Soo Chan KIM

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Country

Republic of Korea

Language

English

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Abstract

No abstract available.

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