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Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.
Kokoszka, Jason E; Waymire, Katrina G; Flierl, Adrian; Sweeney, Katelyn M; Angelin, Alessia; MacGregor, Grant R; Wallace, Douglas C.
Afiliação
  • Kokoszka JE; Forensic Biology Section, Alabama Department of Forensic Sciences, Annex C, Mobile, AL 36617, United States.
  • Waymire KG; Department of Developmental and Cell Biology, University of California Irvine, Irvine, CA 92697-2300, United States.
  • Flierl A; The Parkinson's Institute, Sunnyvale, CA 94085, United States.
  • Sweeney KM; Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
  • Angelin A; Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
  • MacGregor GR; Department of Developmental and Cell Biology, University of California Irvine, Irvine, CA 92697-2300, United States.
  • Wallace DC; Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States. Electronic address: wallaced1@email.chop.edu.
Biochim Biophys Acta ; 1857(8): 1203-1212, 2016 Aug.
Article em En | MEDLINE | ID: mdl-27048932

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article