Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy (1994)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1016/0022-510x(94)90213-5
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the Neurological Sciences
- Volume/Número/Paginação/Ano: v.123, p.122-8, 1994
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ZATZ, Mayana et al. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences, v. 123, p. 122-8, 1994Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(94)90213-5. Acesso em: 19 abr. 2024. -
APA
Zatz, M., Matsumura, K., Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., Marie, S. K. N., & Campbell, K. P. (1994). Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences, 123, 122-8. doi:10.1016/0022-510x(94)90213-5 -
NLM
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Campbell KP. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1994 ;123 122-8.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5 -
Vancouver
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Campbell KP. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1994 ;123 122-8.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5 - Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
- High proportion of new mutations and possible anticipation following molecular genetic studies in brazilian facioscapulohumeral muscular dystrophy (fshd) families
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
- A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
- Mapping, cloning, and characterization of genes important for human development
- Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype
- Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
Informações sobre o DOI: 10.1016/0022-510x(94)90213-5 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
