Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin (2000)
- Authors:
- USP affiliated authors: MARIE, SUELY KAZUE NAGAHASHI - FM ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- DOI: 10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 92, p. 122-7, 2000
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ROCCO, P. et al. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. American Journal of Medical Genetics, v. 92, p. 122-7, 2000Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b. Acesso em: 26 abr. 2024. -
APA
Rocco, P., Vainzof, M., Froehner, S. C., Peters, M. F., Marie, S. K. N., Passos-Bueno, M. R., & Zatz, M. (2000). Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. American Journal of Medical Genetics, 92, 122-7. doi:10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b -
NLM
Rocco P, Vainzof M, Froehner SC, Peters MF, Marie SKN, Passos-Bueno MR, Zatz M. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin [Internet]. American Journal of Medical Genetics. 2000 ; 92 122-7.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b -
Vancouver
Rocco P, Vainzof M, Froehner SC, Peters MF, Marie SKN, Passos-Bueno MR, Zatz M. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin [Internet]. American Journal of Medical Genetics. 2000 ; 92 122-7.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b - Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population
- Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
- Fatores de risco associados à calcinose na dermatomiosite juvenil
- Estudo populacional das ataxias espinocerebelares na população brasileira
- Sarcoglicanopatias na população brasileira
- Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI)
- Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population
- Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex
- Nebulin expression in patients with nemaline myopathy
- Mecanismo molecular da distrofia muscular fácio-escápulo-humeral: ainda uma incógnita!
Informações sobre o DOI: 10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas