Oligospermic infertility associated with an androgen receptor mutation that disrupts interdomain and coactivator (TIF2) interactions

Structural changes in the androgen receptor (AR) are one of the causes of defective spermatogenesis. We screened the AR gene of 173 infertile men with impaired spermatogenesis and identified 3 of them, unrelated, who each had a single adenine→guanine transition that changed codon 886 in exon 8 from...

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Detalhes bibliográficos
Main Authors: Ghadessy, Farid J., Lim, Joyce, Abdullah, Abdullah A.R., Panet-Raymond, Valerie, Choo, Chee Keong, Lumbroso, Rose, Tut, Thein G., Gottlieb, Bruce, Pinsky, Leonard, Trifiro, Mark A., Yong, Eu Leong
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1999
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC408364/
https://ncbi.nlm.nih.gov/pubmed/10359561
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