High frequency of Q318X mutation in patients with...

Arquivos Brasileiros de Endocrinologia & Metabologia 2009 / 02 Vol. 53; Iss. 1

High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil

Campos, Viviane C., Pereira, Rossana M. C., Torres, Natália, Castro, Margaret de, Aguiar-Oliveira, Manuel H.
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Volume:
53
Language:
english
Journal:
Arquivos Brasileiros de Endocrinologia & Metabologia
DOI:
10.1590/s0004-27302009000100007
Date:
February, 2009
File:
PDF, 173 KB
english, 2009
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