Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT (2010)
- Authors:
- Autor USP: REED, UMBERTINA CONTI - FM
- Unidade: FM
- Subjects: NUCLEOTÍDEOS; LIPOSSOMOS; ENZIMAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Biological Chemistry
- ISSN: 0021-9258
- Volume/Número/Paginação/Ano: v. 285, n. 13, p. 10005-10015, 2010
-
ABNT
ZHANG, Rui-Zhu et al. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT. Journal of Biological Chemistry, v. 285, n. 13, p. 10005-10015, 2010Tradução . . Disponível em: http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f. Acesso em: 16 abr. 2024. -
APA
Zhang, R. -Z., Zou, Y., Pan, T. -C., Markova, D., Fertala, A., Hu, Y., et al. (2010). Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT. Journal of Biological Chemistry, 285( 13), 10005-10015. Recuperado de http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f -
NLM
Zhang R-Z, Zou Y, Pan T-C, Markova D, Fertala A, Hu Y, Squarzoni S, Reed UC, Marie SKN, Bönnemann CG, Chu M-L. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT [Internet]. Journal of Biological Chemistry. 2010 ; 285( 13): 10005-10015.[citado 2024 abr. 16 ] Available from: http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f -
Vancouver
Zhang R-Z, Zou Y, Pan T-C, Markova D, Fertala A, Hu Y, Squarzoni S, Reed UC, Marie SKN, Bönnemann CG, Chu M-L. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT [Internet]. Journal of Biological Chemistry. 2010 ; 285( 13): 10005-10015.[citado 2024 abr. 16 ] Available from: http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f - Semiologia neuropediátrica: desenvolvimento neuropsicomotor
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- Inter-relações entre distúrbios respiratórios do sono, respiração bucal e distúrbios do comportamento na infância
- Sindrome da crianca hipotonica
- Toxoplasmose congenita
- Causas neuromusculares de hipotonia
- Miopatias
- Toxoplasmose congenita
- Immunocytochemical study of major histocompatibility complex class I in neuromuscular disorders: the importance on differential diagnosis in inflammatory miopathies
- Desmin and vimentin analysis in nemaline myopathy
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