Androgen Receptor Binding Studies on Heterozygotes in a Family with Androgen Insensitivity Syndrome
โ Scribed by H.E. Maclean; S. Chu; F. Joske; G.L. Warne; J.D. Zajac
- Book ID
- 112238046
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 609 KB
- Volume
- 55
- Category
- Article
- ISSN
- 1077-3150
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๐ SIMILAR VOLUMES
An exonic single nucleotide substitution in the human androgen receptor gene (hAR) could be detected in an Italian family with two children affected by complete androgen insensitivity syndrome (CAIS), also called testicular feminization. This mutation leads to a guanine to adenine transition in exon
Mutations of the androgen receptor gene causing androgen insensitivity syndrome in 46, XY individuals, result in phenotypes ranging from complete female to ambiguous genitalia to males with minor degrees of undervirilization. We studied two Brazilian brothers with partial androgen insensitivity synd