Schmidt, Wolfgang M.; Kraus, Cornelia; Höger, Harald; Oberndorfer, Felicitas; Branka, Manuela; Bingemann, Sonja; Lassmann, Hans; Müller, Markus; Macedo-Souza, Lúcia Inês; Vainzof, Mariz 
; Zatz, Mayana ; Reis, André; Bittner, Reginald E.
Source: EMBO reports. Unidade: IB
Subjects: DOENÇAS NEURODEGENERATIVAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 06 nov. 2024.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.7401001NLM
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 2024 nov. 06 ] Available from: https://doi.org/10.1038/sj.embor.7401001Vancouver
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 2024 nov. 06 ] Available from: https://doi.org/10.1038/sj.embor.7401001
