Spinocerebellar ataxia with hypogonadism: an intriguing group of genetic disorders (2010)
- Authors:
- USP affiliated authors: MARQUES JÚNIOR, WILSON - FMRP ; BARREIRA, AMILTON ANTUNES - FMRP ; SOBREIRA, CLAUDIA FERREIRA DA ROSA - FMRP
- Unidade: FMRP
- Subjects: ATAXIA (RELAÇÃO;ESTUDO); HIPOGONADISMO; DOENÇAS NEUROMUSCULARES; PACIENTES (AVALIAÇÃO)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Inherited Metabolic Disease
- Volume/Número/Paginação/Ano: v. 33, suppl. 1, p. S76, res. 212-P, 2010
- Conference titles: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism
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ABNT
LOURENÇO, C. M. et al. Spinocerebellar ataxia with hypogonadism: an intriguing group of genetic disorders. Journal of Inherited Metabolic Disease. Dordrecht: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 28 mar. 2024. , 2010 -
APA
Lourenço, C. M., Sobreira, C. F. da R., Barreira, A. A., & Marques Júnior, W. (2010). Spinocerebellar ataxia with hypogonadism: an intriguing group of genetic disorders. Journal of Inherited Metabolic Disease. Dordrecht: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Lourenço CM, Sobreira CF da R, Barreira AA, Marques Júnior W. Spinocerebellar ataxia with hypogonadism: an intriguing group of genetic disorders. Journal of Inherited Metabolic Disease. 2010 ; 33 S76.[citado 2024 mar. 28 ] -
Vancouver
Lourenço CM, Sobreira CF da R, Barreira AA, Marques Júnior W. Spinocerebellar ataxia with hypogonadism: an intriguing group of genetic disorders. Journal of Inherited Metabolic Disease. 2010 ; 33 S76.[citado 2024 mar. 28 ] - Late-onset TTRMET30 famial amyloid polyneuropathy (FAPTTRMET30)
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