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Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations.
Roos, S; Lindgren, U; Ehrstedt, C; Moslemi, A R; Oldfors, A.
Afiliación
  • Roos S; Department of Pathology, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden. Electronic address: sara.roos@gu.se.
  • Lindgren U; Department of Pathology, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Ehrstedt C; Department of Women's and Children's Health, Uppsala University Children's Hospital, Uppsala, Sweden.
  • Moslemi AR; Department of Pathology, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Oldfors A; Department of Pathology, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Neuromuscul Disord ; 24(8): 713-20, 2014 Aug.
Article en En | MEDLINE | ID: mdl-24953930
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Timidina Quinasa / ADN Mitocondrial / Miopatías Mitocondriales / Fibras Musculares Esqueléticas Límite: Child, preschool / Humans / Male Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Reino Unido
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Timidina Quinasa / ADN Mitocondrial / Miopatías Mitocondriales / Fibras Musculares Esqueléticas Límite: Child, preschool / Humans / Male Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Reino Unido