Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family (2000)
- Autores:
- Autores USP: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-#
- Assunto: GENÉTICA MÉDICA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Muscle & Nerve
- ISSN: 0148-639X
- Volume/Número/Paginação/Ano: v. 23, p. 984-988, jun. 2000
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
VAINZOF, Mariz et al. Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family. Muscle & Nerve, v. 23, n. ju 2000, p. 984-988, 2000Tradução . . Disponível em: https://doi.org/10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-#. Acesso em: 19 abr. 2024. -
APA
Vainzof, M., Moreira, E. S., Canovas, M., Anderson, L. V. B., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2000). Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family. Muscle & Nerve, 23( ju 2000), 984-988. doi:10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-# -
NLM
Vainzof M, Moreira ES, Canovas M, Anderson LVB, Pavanello R de CM, Passos-Bueno MR, Zatz M. Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family [Internet]. Muscle & Nerve. 2000 ; 23( ju 2000): 984-988.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-# -
Vancouver
Vainzof M, Moreira ES, Canovas M, Anderson LVB, Pavanello R de CM, Passos-Bueno MR, Zatz M. Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family [Internet]. Muscle & Nerve. 2000 ; 23( ju 2000): 984-988.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-# - 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: 10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-# (Fonte: oaDOI API)
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas