Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population (1999)
- Authors:
- USP affiliated authors: MARIE, SUELY KAZUE NAGAHASHI - FM ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- DOI: 10.1016/s0022-510x(99)00040-4
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Estados Unidos
- Date published: 1999
- 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: 29 dez. 2025. -
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., Oliveira, A. S. B., Zatz, M., & Marie, S. K. N. (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 RCM, Oliveira ASB, Zatz M, Marie SKN. 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. 29 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4 -
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello RCM, Oliveira ASB, Zatz M, Marie SKN. 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. 29 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4 - Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin
- Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
- 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 molecular da neuropatia de Charcot-Marie-Tooth tipo 1 (CMT1) e neuropatia hereditária com paralisias por compressão (HNPP)
- Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy
- Rods proteic-constituition and muscle fiber maturation in nemaline myopathy
- Estudo populacional das ataxias espinocerebelares na população brasileira
- Sarcoglicanopatias na população brasileira
Informações sobre o DOI: 10.1016/s0022-510x(99)00040-4 (Fonte: oaDOI API)
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