Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration (2007)
- Authors:
- USP affiliated authors: VAINZOF, MARIZ - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1038/sj.embor.7401001
- Subjects: DOENÇAS NEURODEGENERATIVAS; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: EMBO reports
- ISSN: 1469-221X
- Volume/Número/Paginação/Ano: v. 8, n. 7, p. 691-697, 2007
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
SCHMIDT, Wolfgang M. et al. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO reports, v. 8, n. 7, p. 691-697, 2007Tradução . . Disponível em: https://doi.org/10.1038/sj.embor.7401001. Acesso em: 25 jan. 2026. -
APA
Schmidt, W. M., Kraus, C., Höger, H., Oberndorfer, F., Branka, M., Bingemann, S., et al. (2007). Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO reports, 8( 7), 691-697. doi:10.1038/sj.embor.7401001 -
NLM
Schmidt WM, Kraus C, Höger H, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration [Internet]. EMBO reports. 2007 ; 8( 7): 691-697.[citado 2026 jan. 25 ] Available from: https://doi.org/10.1038/sj.embor.7401001 -
Vancouver
Schmidt WM, Kraus C, Höger H, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration [Internet]. EMBO reports. 2007 ; 8( 7): 691-697.[citado 2026 jan. 25 ] Available from: https://doi.org/10.1038/sj.embor.7401001 - The 10 autosomal recessive limb-girdle muscular dystrophies
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Informações sobre o DOI: 10.1038/sj.embor.7401001 (Fonte: oaDOI API)
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