A gene for universal congenital alopecia maps to chromosome 8p21-22.

Complete or partial congenital absence of hair (congenital alopecia) may occur either in isolation or with associated defects. The majority of families with isolated congenital alopecia has been reported to follow an autosomal-recessive mode of inheritance (MIM 203655). As yet, no gene has been link...

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Autors principals: Nöthen, M M, Cichon, S, Vogt, I R, Hemmer, S, Kruse, R, Knapp, M, Höller, T, Faiyaz ul Haque, M, Haque, S, Propping, P, Ahmad, M, Rietschel, M
Format: Artigo
Idioma:Inglês
Publicat: 1998
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1376893/
https://ncbi.nlm.nih.gov/pubmed/9463324
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