Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes (2000)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidade: IB
- DOI: 10.1097/00019052-200010000-00002
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2000
- Source:
- Título do periódico: Current Opinion in Neurology
- Volume/Número/Paginação/Ano: v. 13, p. 511-517, oct. 2000
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ZATZ, Mayana e VAINZOF, Mariz e PASSOS-BUENO, Maria Rita. Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes. Current Opinion in Neurology, v. 13, p. 511-517, 2000Tradução . . Disponível em: https://doi.org/10.1097/00019052-200010000-00002. Acesso em: 23 abr. 2024. -
APA
Zatz, M., Vainzof, M., & Passos-Bueno, M. R. (2000). Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes. Current Opinion in Neurology, 13, 511-517. doi:10.1097/00019052-200010000-00002 -
NLM
Zatz M, Vainzof M, Passos-Bueno MR. Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes [Internet]. Current Opinion in Neurology. 2000 ; 13 511-517.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1097/00019052-200010000-00002 -
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR. Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes [Internet]. Current Opinion in Neurology. 2000 ; 13 511-517.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1097/00019052-200010000-00002 - 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: 10.1097/00019052-200010000-00002 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
