Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients (2000)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v. 67, n. 4, suppl. 2, p. 251, Oct. 2000
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
PAULA, F et al. Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 2000 -
APA
Paula, F., Moreira, E. S., Bernadino, A. L. F., Kai, A., Passos-Bueno, M. R., Vainzof, M., & Zatz, M. (2000). Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. -
NLM
Paula F, Moreira ES, Bernadino ALF, Kai A, Passos-Bueno MR, Vainzof M, Zatz M. Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. 2000 ; 67( 4): 251.[citado 2024 abr. 19 ] -
Vancouver
Paula F, Moreira ES, Bernadino ALF, Kai A, Passos-Bueno MR, Vainzof M, Zatz M. Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. 2000 ; 67( 4): 251.[citado 2024 abr. 19 ] - 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas