Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy (1993)
- Authors:
- USP affiliated authors: LEVY, JOSE ANTONIO - FM ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Canadian Journal of Neurological Sciences
- Volume/Número/Paginação/Ano: v.20, n.suppl.4, p.s30, aug. 1993
- Conference titles: World Congress of Neurology
-
ABNT
PASSOS-BUENO, Maria Rita et al. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 29 dez. 2025. , 1993 -
APA
Passos-Bueno, M. R., Cerqueira, A., Takata, R. I., Pavanello, R. C. M., Eggers, S., Marie, S. K. N., et al. (1993). Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Passos-Bueno MR, Cerqueira A, Takata RI, Pavanello RCM, Eggers S, Marie SKN, Levy JA, Zatz M. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2025 dez. 29 ] -
Vancouver
Passos-Bueno MR, Cerqueira A, Takata RI, Pavanello RCM, Eggers S, Marie SKN, Levy JA, Zatz M. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2025 dez. 29 ] - Brazilian family with 3271 mutation in mitochondrial dna
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- Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages
- Variacao do quadro clinico da distrofia fascio-escapulo-umeral em 31 familias brasileiras (resumo)
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
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