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Response to "In silico prediction is insufficient to assess pathogenicity of mtDNA variants".
Bacalhau, Mafalda; Pratas, João; Simões, Marta; Mendes, Cândida; Ribeiro, Carolina; Santos, Maria J; Diogo, Luisa; Macário, Maria Carmo; Grazina, Manuela.
Afiliação
  • Bacalhau M; Faculty of Medicine, University of Coimbra, PA 3000-354, Portugal; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal.
  • Pratas J; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal.
  • Simões M; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal.
  • Mendes C; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal.
  • Ribeiro C; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal.
  • Santos MJ; Faculty of Medicine, University of Coimbra, PA 3000-354, Portugal; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal.
  • Diogo L; Pediatric Hospital of Coimbra - CHUC EPE, Portugal.
  • Macário MC; Neurology Department, Coimbra University Hospitals - CHUC EPE, Portugal.
  • Grazina M; Faculty of Medicine, University of Coimbra, PA 3000-354, Portugal; Center for Neuroscience and Cell Biology, University of Coimbra - Laboratory of Biochemical Genetics, Portugal. Electronic address: mgrazina.fmuc@gmail.com.
Eur J Med Genet ; 61(1): 46-47, 2018 01.
Article em En | MEDLINE | ID: mdl-28807868

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mitocôndrias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Eur J Med Genet Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mitocôndrias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Eur J Med Genet Ano de publicação: 2018 Tipo de documento: Article