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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Vydáno v:Ann Transl Med
Hlavní autoři: Dung, Vu Chi, Fukami, Maki, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Nga, Pham Thu, Dat, Nguyen Phu, Ogata, Tsutomu
Médium: Artigo
Jazyk:Inglês
Vydáno: AME Publishing Company 2015
Témata:
Part 4: Oral/poster
On-line přístup: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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