Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome

Ana Paula Abreu Ericka Barbosa Trarbach; Margaret de Castro; Elaine Maria Frade Costa; Beatriz Versiani; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 93, n. 10, p. 4113-4118, 2008

Philadelphia 2008

Localização: FM - Fac. Medicina    (BCSEP 230 2008 ) e outros locais(Acessar)