Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population (1999)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidades: IB; FM
- DOI: 10.1016/s0022-510x(99)00040-4
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of the Neurological Sciences
- Volume/Número/Paginação/Ano: v. 164, p. 44-49, 1999
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
VAINZOF, Mariz et al. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. Journal of the Neurological Sciences, v. 164, p. 44-49, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0022-510x(99)00040-4. Acesso em: 27 dez. 2025. -
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. de C. M., Marie, S. K. N., Oliveira, A. B. S., & Zatz, M. (1999). Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. Journal of the Neurological Sciences, 164, 44-49. doi:10.1016/s0022-510x(99)00040-4 -
NLM
Vainzof M, Passos-Bueno MR, Pavanello R de CM, Marie SKN, Oliveira ABS, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population [Internet]. Journal of the Neurological Sciences. 1999 ; 164 44-49.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4 -
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello R de CM, Marie SKN, Oliveira ABS, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population [Internet]. Journal of the Neurological Sciences. 1999 ; 164 44-49.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4 - Estudo molecular de neuropatias periféricas - CMT1A e HNPP
- The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype
- Estudo molecular da neuropatia de Charcot-Marie-Tooth tipo 1 (CMT1) e neuropatia hereditária com paralisias por compressão (HNPP)
- Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1
- A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies
- The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis
- Estudo populacional das ataxias espinocerebelares na população brasileira
- Sarcoglicanopatias na população brasileira
- Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI)
- Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex
Informações sobre o DOI: 10.1016/s0022-510x(99)00040-4 (Fonte: oaDOI API)
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