Mutations of androgen receptor gene in Brazilian patients with male pseudohermaphroditism


Autoria(s): Cabral,D.F.; Maciel-Guerra,A.T.; Hackel,C.
Data(s)

01/06/1998

Resumo

We describe the identification of point mutations in the androgen receptor gene in five Brazilian patients with female assignment and behavior. The eight exons of the gene were amplified by the polymerase chain reaction (PCR) and analyzed for single-strand conformation polymorphism (SSCP) to detect the mutations. Direct sequencing of the mutant PCR products demonstrated single transitions in three of these cases: G<FONT FACE="Symbol">®</font>A in case 1, within exon C, changing codon 615 from Arg to His; G<FONT FACE="Symbol">®</font>A in case 2, within exon E, changing codon 752 from Arg to Gln, and C<FONT FACE="Symbol">®</font>T in case 3, within exon B, but without amino acid change.

Formato

text/html

Identificador

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000600008

Idioma(s)

en

Publicador

Associação Brasileira de Divulgação Científica

Fonte

Brazilian Journal of Medical and Biological Research v.31 n.6 1998

Palavras-Chave #androgen receptor gene #gene mutations #androgen insensitivity syndromes #male pseudohermaphroditism
Tipo

journal article