Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients (2001)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Assunto: DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v. 69, n. 4, suppl., p. 442, oct. 2001
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
VAGENAS, Dulci do Nascimento Fonseca et al. Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2001 -
APA
Vagenas, D. do N. F., Cerqueira, A., Torres, A., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2001). Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. -
NLM
Vagenas D do NF, Cerqueira A, Torres A, Pavanello R de CM, Passos-Bueno MR, Zatz M. Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. 2001 ; 69( 4): 442.[citado 2024 abr. 27 ] -
Vancouver
Vagenas D do NF, Cerqueira A, Torres A, Pavanello R de CM, Passos-Bueno MR, Zatz M. Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. 2001 ; 69( 4): 442.[citado 2024 abr. 27 ] - Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- 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
- Mutations in the proteolytic enzyme calpain 3 cause lim-girdle muscular dystrophy type 2a
- Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)
- Ausencia de heterogeneidade genetica na distrofia muscular tipo facio-escapulo-humeral (fsh) atraves de estudos de ligacao
- Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene
- Delecoes no gene da distrofina em pacientes com distrofia muscular de duchenne e becker
- Distrofias musculares progressivas: os novos caminhos apos a descoberta da distrofia
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
