Intragenic deletion mutation in the gene desmoglein 4 underlies autosomal recessive hypotrichosis in six consanguineous families

Dost, Muhammad; Bushra, Khan; Syed I., Raza; Farooq, Ahmad; Naseem A., Channa; Muhammad, Ansar; Wasim, Ahmad; Sulman, Basit

Dost, Muhammad; Bushra, Khan; Syed I., Raza; Farooq, Ahmad; Naseem A., Channa; Muhammad, Ansar; Wasim, Ahmad; Sulman, Basit.

Journal of Taibah University Medical Sciences. 2016; 11 (3): 203-210

in En | IMEMR | ID: emr-180219

Responsible library: EMRO

Subject(s)

Humans; Sequence Deletion; Genetic Association Studies; Desmogleins/genetics; Consanguinity

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Index: IMEMR Main subject: Sequence Deletion / Consanguinity / Desmogleins / Genetic Association Studies Limits: Humans Language: En Journal: J. Taibah Univ. Med. Sci. Year: 2016

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