Source: Human Molecular Genetics. Unidades: ICB, FM, IB
Subjects: DOENÇAS NEURODEGENERATIVAS, SEQUENCIAMENTO GENÉTICO, DOENÇAS GENÉTICAS, MAPEAMENTO GENÉTICO, NEUROGENÉTICA, HEREDITARIEDADE, REPARAÇÃO DE DNA
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MELO, Uira S et al. Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome. Human Molecular Genetics, p. 1-9, 2015Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddv388. Acesso em: 27 ago. 2024.APA
Melo, U. S., Macedo-Souza, L. I., Figueiredo, T., Muotri, A. R., Gleeson,, Coux, G., et al. (2015). Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome. Human Molecular Genetics, 1-9. doi:10.1093/hmg/ddv388NLM
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson, Coux G, Armas P, Calcaterra NB, Kitajima JP, Amorim S, Olávio TR, Griesi-Oliveira K, Coatti GC, Rocha CRR, Martins-Pinheiro M, Menck CFM, Zaki MS, Kok F, Zatz M, Santos S. Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome [Internet]. Human Molecular Genetics. 2015 ; 1-9.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1093/hmg/ddv388Vancouver
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson, Coux G, Armas P, Calcaterra NB, Kitajima JP, Amorim S, Olávio TR, Griesi-Oliveira K, Coatti GC, Rocha CRR, Martins-Pinheiro M, Menck CFM, Zaki MS, Kok F, Zatz M, Santos S. Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome [Internet]. Human Molecular Genetics. 2015 ; 1-9.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1093/hmg/ddv388