A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 (2004)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; VAINZOF, MARIZ - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1038/sj.ejhg.5201289
- Assunto: DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: European Journal of Human Genetics
- ISSN: 1018-4813
- Volume/Número/Paginação/Ano: v. 12, n. 12, p. 1033-1040, 2004
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
STARLING, Alessandra et al. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. European Journal of Human Genetics, v. 12, n. 12, p. 1033-1040, 2004Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201289. Acesso em: 18 abr. 2024. -
APA
Starling, A., Kok, F., Passos-Bueno, M. R., Vainzof, M., & Zatz, M. (2004). A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. European Journal of Human Genetics, 12( 12), 1033-1040. doi:10.1038/sj.ejhg.5201289 -
NLM
Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 [Internet]. European Journal of Human Genetics. 2004 ; 12( 12): 1033-1040.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1038/sj.ejhg.5201289 -
Vancouver
Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 [Internet]. European Journal of Human Genetics. 2004 ; 12( 12): 1033-1040.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1038/sj.ejhg.5201289 - Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation?
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Informações sobre o DOI: 10.1038/sj.ejhg.5201289 (Fonte: oaDOI API)
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