A gene related to Caenorhabditis elegans spermatogenes is factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B (1998)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1038/1689
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Nature Genetics
- Volume/Número/Paginação/Ano: v. 20, p. 37-42, set. 1998
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
BASHIR, Rumaisa et al. A gene related to Caenorhabditis elegans spermatogenes is factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nature Genetics, v. 20, p. 37-42, 1998Tradução . . Disponível em: https://doi.org/10.1038/1689. Acesso em: 29 dez. 2025. -
APA
Bashir, R., Britton, S., Strachan, T., Keers, S., Vafiadaki, E., Lako, M., et al. (1998). A gene related to Caenorhabditis elegans spermatogenes is factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nature Genetics, 20, 37-42. doi:10.1038/1689 -
NLM
Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, Lako M, Richard I, Marchand S, Bourg N, Argov Z, Sadeh M, Mahjneh I, Marconi G, Passos-Bueno MR, Moreira E de S, Zatz M, Beckmann JS, Bushby K. A gene related to Caenorhabditis elegans spermatogenes is factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B [Internet]. Nature Genetics. 1998 ; 20 37-42.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1038/1689 -
Vancouver
Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, Lako M, Richard I, Marchand S, Bourg N, Argov Z, Sadeh M, Mahjneh I, Marconi G, Passos-Bueno MR, Moreira E de S, Zatz M, Beckmann JS, Bushby K. A gene related to Caenorhabditis elegans spermatogenes is factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B [Internet]. Nature Genetics. 1998 ; 20 37-42.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1038/1689 - 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
- 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
Informações sobre o DOI: 10.1038/1689 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
