Caucasian family with the 3271 mutation in mitochondrial dna (1994)
- 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: Biochemical Medicine and Metabolic Biology
- Volume/Número/Paginação/Ano: v.52, p.136-9, 1994
-
ABNT
MARIE, Suely Kazue Nagahashi et al. Caucasian family with the 3271 mutation in mitochondrial dna. Biochemical Medicine and Metabolic Biology, v. 52, p. 136-9, 1994Tradução . . Acesso em: 16 out. 2024. -
APA
Marie, S. K. N., Goto, Y. C., Passos-Bueno, M. R., Zatz, M., Carvalho, A. A. S., Carvalho, M. S., et al. (1994). Caucasian family with the 3271 mutation in mitochondrial dna. Biochemical Medicine and Metabolic Biology, 52, 136-9. -
NLM
Marie SKN, Goto YC, Passos-Bueno MR, Zatz M, Carvalho AAS, Carvalho MS, Levy JA, Palou VSEB, Campiotto S, Horai S, Nonaka I. Caucasian family with the 3271 mutation in mitochondrial dna. Biochemical Medicine and Metabolic Biology. 1994 ;52 136-9.[citado 2024 out. 16 ] -
Vancouver
Marie SKN, Goto YC, Passos-Bueno MR, Zatz M, Carvalho AAS, Carvalho MS, Levy JA, Palou VSEB, Campiotto S, Horai S, Nonaka I. Caucasian family with the 3271 mutation in mitochondrial dna. Biochemical Medicine and Metabolic Biology. 1994 ;52 136-9.[citado 2024 out. 16 ] - Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy
- Brazilian family with 3271 mutation in mitochondrial dna
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- Distrofina nas distrofias musculares progressivas
- Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Variacao do quadro clinico da distrofia fascio-escapulo-umeral em 31 familias brasileiras (resumo)
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