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Application of Genome Sequencing from Blood to Diagnose Mitochondrial Diseases.
Rius, Rocio; Compton, Alison G; Baker, Naomi L; Welch, AnneMarie E; Coman, David; Kava, Maina P; Minoche, Andre E; Cowley, Mark J; Thorburn, David R; Christodoulou, John.
Afiliação
  • Rius R; Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia.
  • Compton AG; Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia.
  • Baker NL; Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia.
  • Welch AE; Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia.
  • Coman D; Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia.
  • Kava MP; Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia.
  • Minoche AE; Victorian Clinical Genetic Services, Melbourne, VIC 3052, Australia.
  • Cowley MJ; Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia.
  • Thorburn DR; Department of Metabolic Medicine, Queensland Children's Hospital, Brisbane, QLD 4101, Australia.
  • Christodoulou J; School of Clinical Medicine, University of Queensland, Brisbane, QLD 4072, Australia.
Genes (Basel) ; 12(4)2021 04 20.
Article em En | MEDLINE | ID: mdl-33924034
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / DNA / Doenças Mitocondriais / Sequenciamento Completo do Genoma Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Adolescent / Child, preschool / Female / Humans / Male Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / DNA / Doenças Mitocondriais / Sequenciamento Completo do Genoma Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Adolescent / Child, preschool / Female / Humans / Male Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article