A novel complex neurological phenotype due to a homozygous mutation in FDX2 (2018)
Subjects: FENÓTIPOS, MIOPATIAS CONGÊNITAS ESTRUTURAIS, ATROFIA MUSCULAR, SEQUENCIAMENTO GENÉTICO, IMAGEM POR RESSONÂNCIA MAGNÉTICA
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GURGEL-GIANNETTI, Juliana e KOK, Fernando. A novel complex neurological phenotype due to a homozygous mutation in FDX2. Brain, v. 141, p. 2289-2298, 2018Tradução . . Disponível em: https://doi.org/10.1093/brain/awy172. Acesso em: 09 nov. 2024.APA
Gurgel-giannetti, J., & Kok, F. (2018). A novel complex neurological phenotype due to a homozygous mutation in FDX2. Brain, 141, 2289-2298. doi:10.1093/brain/awy172NLM
Gurgel-giannetti J, Kok F. A novel complex neurological phenotype due to a homozygous mutation in FDX2 [Internet]. Brain. 2018 ; 141 2289-2298.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/brain/awy172Vancouver
Gurgel-giannetti J, Kok F. A novel complex neurological phenotype due to a homozygous mutation in FDX2 [Internet]. Brain. 2018 ; 141 2289-2298.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/brain/awy172
