Complete form of androgen insensitivity syndrome in Brazilian patients due to P766A mutation in the androgen receptor;Insensibilidade completa aos andrógenos em pacientes brasileiras causada pela mutação P766A no gene do receptor androgênico.

Arquivos brasileiros de endocrinologia e metabologia

Volumn 49, Issue 1, 2005, Pages 98-102

  Corrêa, Rafaela V ^a   Wey, João C ^a   Billerbeck, Ana E C ^a   Melo, Karla F S ^a   Mendonça, Berenice B ^a   Wey, Marta V ^a   Arnhold, Ivo J P ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

ANDROGEN INSENSITIVITY SYNDROME; ARTICLE; BRAZIL; FEMALE; GENETICS; HUMAN; KARYOTYPING; MALE; MUTATION; TWINS;

ANDROGEN-INSENSITIVITY SYNDROME; BRAZIL; DISEASES IN TWINS; FEMALE; HUMANS; KARYOTYPING; MALE; MUTATION; RECEPTORS, ANDROGEN;

MLCS; MLOWN;

EID: 33745559441     PISSN: 00042730     EISSN: None     Source Type: Journal    
DOI: 10.1590/s0004-27302005000100013     Document Type: Article

References (0)