Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.

Kruse, R; Cichon, S; Anker, M; Hillmer, A M; Barros-Núñez, P; Cantú, J M; Leal, E; Weinlich, G; Schmuth, M; Fritsch, P; Ruzicka, T; Propping, P; Nöthen, M M

Kruse, R; Cichon, S; Anker, M; Hillmer, A M; Barros-Núñez, P; Cantú, J M; Leal, E; Weinlich, G; Schmuth, M; Fritsch, P; Ruzicka, T; Propping, P; Nöthen, M M.

Affiliation

Kruse R; Institute of Human Genetics, University of Bonn, Germany.

J Invest Dermatol ; 113(6): 954-9, 1999 Dec.

Article in En | MEDLINE | ID: mdl-10594736

Subject(s)

Alopecia/congenital; Alopecia/genetics; Frameshift Mutation; Mutation, Missense; Adult; Female; Humans; Male; Polymorphism, Genetic

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Collection: 01-internacional Database: MEDLINE Main subject: Frameshift Mutation / Mutation, Missense / Alopecia Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: J Invest Dermatol Year: 1999 Type: Article Affiliation country: Germany

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