Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia.

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Source: The British Journal of Dermatology - March 11, 2018 Category: Dermatology Authors: Intarak N, Theerapanon T, Srijunbarl A, Suphapeetiporn K, Porntaveetus T, Shotelersuk V Tags: Br J Dermatol Source Type: research