A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype (1998)
- Authors:
- USP affiliated authors: ABELIN, NEUSA MARIA ALVES - FM ; TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: MEDICINA INTERNA
- Language: Inglês
- Source:
- Título do periódico: Molecular Endocrinology
- Volume/Número/Paginação/Ano: v. 12, n. 6, p. 775-784, 1998
-
ABNT
MARTENS, John W. M et al. A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology, v. 12, n. 6, p. 775-784, 1998Tradução . . Acesso em: 21 maio 2024. -
APA
Martens, J. W. M., Post, M. V., Abelin, N. M. A., Ezabella, M., Toledo, S. P. A., Brunner, H. G., & Themmen, A. P. N. (1998). A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology, 12( 6), 775-784. -
NLM
Martens JWM, Post MV, Abelin NMA, Ezabella M, Toledo SPA, Brunner HG, Themmen APN. A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology. 1998 ; 12( 6): 775-784.[citado 2024 maio 21 ] -
Vancouver
Martens JWM, Post MV, Abelin NMA, Ezabella M, Toledo SPA, Brunner HG, Themmen APN. A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology. 1998 ; 12( 6): 775-784.[citado 2024 maio 21 ] - Familial acromegaly (fa) not associated to multiple endocrine neoplasia type - 1 (mfm - 1)
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