Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype (1994)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: GENÉTICA MÉDICA; NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Muscle and Nerve
- Volume/Número/Paginação/Ano: n.suppl.1, p.s175, 1994
- Conference titles: International Congress Neuromuscular Diseases
-
ABNT
PASSOS-BUENO, Maria Rita et al. Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype. Muscle and Nerve. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1994 -
APA
Passos-Bueno, M. R., Vainzof, M., Marie, S. K. N., & Zatz, M. (1994). Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype. Muscle and Nerve. New York: Instituto de Biociências, Universidade de São Paulo. -
NLM
Passos-Bueno MR, Vainzof M, Marie SKN, Zatz M. Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype. Muscle and Nerve. 1994 ;(suppl.1): s175.[citado 2024 abr. 19 ] -
Vancouver
Passos-Bueno MR, Vainzof M, Marie SKN, Zatz M. Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype. Muscle and Nerve. 1994 ;(suppl.1): s175.[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
- 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)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas