An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity

We have discovered in the X-linked androgen receptor gene a single exonic nucleotide substitution that causes complete androgen insensitivity (resistance) in a sibship with three affected individuals. The mutation, a guanine-to-adenine transition, occurs at nucleotide number 2682 and changes the sen...

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Detalhes bibliográficos
Main Authors: Sai, Tetsujun, Seino, Susumu, Chang, Chawnshang, Trifiro, Mark, Pinsky, Leonard, Mhatre, Anand, Kaufman, Morris, Lambert, Bernard, Trapman, Jan, Brinkmann, Albert O., Rosenfield, Robert L., Liao, Shutsung
Formato: Artigo
Idioma:English
Publicado em: 1990
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683844/
https://ncbi.nlm.nih.gov/pubmed/2339702
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https://ncbi.nlm.nih.gov/pmc/articles/PMC1683844/
https://ncbi.nlm.nih.gov/pubmed/2339702

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