Positional cloning of a gene for autosomal recessive limb-girdle muscular dystrophy (1995)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: GENÉTICA MÉDICA; NEUROLOGIA
- Language: Inglês
- Imprenta:
- Conference titles: European Neuro Muscular Centre International Workshop
-
ABNT
BASHIR, R et al. Positional cloning of a gene for autosomal recessive limb-girdle muscular dystrophy. 1995, Anais.. Naarden: Instituto de Biociências, Universidade de São Paulo, 1995. . Acesso em: 09 out. 2024. -
APA
Bashir, R., Stracham, T., Keers, S., Mahjneh, I., Marconi, G., Passos-Bueno, M. R., et al. (1995). Positional cloning of a gene for autosomal recessive limb-girdle muscular dystrophy. In . Naarden: Instituto de Biociências, Universidade de São Paulo. -
NLM
Bashir R, Stracham T, Keers S, Mahjneh I, Marconi G, Passos-Bueno MR, Zatz M, Bushby K. Positional cloning of a gene for autosomal recessive limb-girdle muscular dystrophy. 1995 ;[citado 2024 out. 09 ] -
Vancouver
Bashir R, Stracham T, Keers S, Mahjneh I, Marconi G, Passos-Bueno MR, Zatz M, Bushby K. Positional cloning of a gene for autosomal recessive limb-girdle muscular dystrophy. 1995 ;[citado 2024 out. 09 ] - Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- 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
- Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd)
- Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy
- Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas