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 do periódico: 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 . . Acesso em: 27 mar. 2023. -
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. Nature Genetics. 1998 ; 20 37-42.[citado 2023 mar. 27 ] -
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. Nature Genetics. 1998 ; 20 37-42.[citado 2023 mar. 27 ] - Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- 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
- Reevalutation and fine mapping of a Brazilian pedigree reveals another family with Allan-Herndon-Dudley syndrome
- Anticipation revisited in facioscapulohumeral muscular dystrophy
- Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor]
- Transposon-like element in the dystrophin gene. [Carta ao editor]
- Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights
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
