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Intragenic deletion mutation in the gene desmoglein 4 underlies autosomal recessive hypotrichosis in six consanguineous families
Journal of Taibah University Medical Sciences. 2016; 11 (3): 203-210
em Inglês | IMEMR (Mediterrâneo Oriental) | ID: emr-180219
Biblioteca responsável: EMRO
ABSTRACT

Objectives:

Localized autosomal recessive hypotrichosis is a non-syndromic human hair loss disorder, affecting scalp, eyebrows and eyelashes, and other parts of the body. Six consanguineous families with this form of hair loss disorder were investigated at both the clinical and molecular levels
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Deleção de Sequência / Consanguinidade / Desmogleínas / Estudos de Associação Genética Limite: Humanos Idioma: Inglês Revista: J. Taibah Univ. Med. Sci. Ano de publicação: 2016