Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? (1995)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1093/hmg/4.3.401
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Human Molecular Genetics
- Volume/Número/Paginação/Ano: v.4 , n.3 , p.401-6, 1995
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ZATZ, Mayana et al. Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?. Human Molecular Genetics, v. 4 , n. 3 , p. 401-6, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.3.401. Acesso em: 24 abr. 2024. -
APA
Zatz, M., Passos-Bueno, M. R., Cerqueira, A. M. P., Marie, S. K. N., Vainzof, M., & Pavanello, R. C. M. (1995). Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? Human Molecular Genetics, 4 ( 3 ), 401-6. doi:10.1093/hmg/4.3.401 -
NLM
Zatz M, Passos-Bueno MR, Cerqueira AMP, Marie SKN, Vainzof M, Pavanello RCM. Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? [Internet]. Human Molecular Genetics. 1995 ;4 ( 3 ): 401-6.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1093/hmg/4.3.401 -
Vancouver
Zatz M, Passos-Bueno MR, Cerqueira AMP, Marie SKN, Vainzof M, Pavanello RCM. Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? [Internet]. Human Molecular Genetics. 1995 ;4 ( 3 ): 401-6.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1093/hmg/4.3.401 - 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
- 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
- Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd)
- Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy
Informações sobre o DOI: 10.1093/hmg/4.3.401 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
