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Congenital Hypermetabolism and Uncoupled Oxidative Phosphorylation.
Ganetzky, Rebecca D; Markhard, Andrew L; Yee, Irene; Clever, Sheila; Cahill, Alan; Shah, Hardik; Grabarek, Zenon; To, Tsz-Leung; Mootha, Vamsi K.
Afiliación
  • Ganetzky RD; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Markhard AL; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Yee I; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Clever S; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Cahill A; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Shah H; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Grabarek Z; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • To TL; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
  • Mootha VK; From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute
N Engl J Med ; 387(15): 1395-1403, 2022 10 13.
Article en En | MEDLINE | ID: mdl-36239646
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fosforilación Oxidativa / Consumo de Oxígeno / Enfermedades Mitocondriales / ATPasas de Translocación de Protón Mitocondriales Límite: Humans / Male Idioma: En Revista: N Engl J Med Año: 2022 Tipo del documento: Article
Texto completo
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XML
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fosforilación Oxidativa / Consumo de Oxígeno / Enfermedades Mitocondriales / ATPasas de Translocación de Protón Mitocondriales Límite: Humans / Male Idioma: En Revista: N Engl J Med Año: 2022 Tipo del documento: Article