AB071. Mutations of AR gene in Vietnamese patients: genotype and phenotype

Androgen insensitivity syndrome (AIS) is the most common specific cause of 46,XY disorder in sex development. The androgen signaling pathway is complex but so far, the only gene linked with AIS is the androgen receptor (AR). Mutations in the AR are found in most subjects with complete AIS but in par...

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Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Dung, Vu Chi, Fukami, Maki, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Nga, Pham Thu, Dat, Nguyen Phu, Ogata, Tsutomu
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2015
Assuntos:
Part 4: Oral/poster
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563444/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB071
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