Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy (1994)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- School: IB
- DOI: 10.1093/hmg/3.6.919
- Subject: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Human Molecular Genetics
- Volume/Número/Paginação/Ano: v.3 , n.6 , p.919-22, 1994
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
PASSOS-BUENO, M R; VAINZOF, M; MARIE, Suely Kazue Nagahashi; ZATZ, M. Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy. Human Molecular Genetics, Oxford, v. 3 , n. 6 , p. 919-22, 1994. DOI: 10.1093/hmg/3.6.919. -
APA
Passos-Bueno, M. R., Vainzof, M., Marie, S. K. N., & Zatz, M. (1994). Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy. Human Molecular Genetics, 3 ( 6 ), 919-22. doi:10.1093/hmg/3.6.919 -
NLM
Passos-Bueno MR, Vainzof M, Marie SKN, Zatz M. Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy. Human Molecular Genetics. 1994 ;3 ( 6 ): 919-22. -
Vancouver
Passos-Bueno MR, Vainzof M, Marie SKN, Zatz M. Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy. Human Molecular Genetics. 1994 ;3 ( 6 ): 919-22. - Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
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- Localizacao de genes responsaveis pelas distrofias musculares tipo cinturas atraves de microsatelites
- Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd)
- Comparison of dystrophin analyses in patients with duchenne muscular dystrophy (dmd) by immunofluorescence (if) and western-blot (wb) tecniques
- Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies
- Dystrophin abnormalities in muscle from becker muscular dystrophy (bmd) carriers
- Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk
Informações sobre o DOI: 10.1093/hmg/3.6.919 (Fonte: oaDOI API)
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