Desmoglein 4 Mutation Underlies Autosomal Recessive Keratosis Pilaris Atrophicans
نویسندگان
چکیده
منابع مشابه
A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis.
Celia Moss*, Amalia Martinez-Mir†, HaMut Lam†, Marija Tadin-Strapps†, Ana Kljuic and Angela M Christiano† *Department of Dermatology, Birmingham Children's Hospital NHS Trust, Birmingham, UK †Departments of Dermatology and Genetics and Development, Columbia University, New York, New York Correspondence: Angela M. Christiano, PhD, Department of Dermatology, Columbia University, College of Physic...
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ژورنال
عنوان ژورنال: Acta Dermato Venereologica
سال: 2018
ISSN: 0001-5555
DOI: 10.2340/00015555-2976