Genetic Diagnosis of Kindler Syndrome, a Rare form of Genodermatosis in a Newborn with Identification of a Nonsense Mutation, c. 328C > T, in the FERMT1 Gene in the Indian Population.
作者信息
Srikumar Afshan, Lava Chaitra, Udumudi Anuradha
机构信息
From the Department of Molecular Genetics, GeneTech, Hyderabad, India E-mail:
出版信息
Indian J Dermatol. 2023 May-Jun;68(3):334-336. doi: 10.4103/ijd.ijd_1034_20.
Abstract
摘要
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