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Defining functional classes of Barth syndrome mutation in humans.
Lu, Ya-Wen; Galbraith, Laura; Herndon, Jenny D; Lu, Ya-Lin; Pras-Raves, Mia; Vervaart, Martin; Van Kampen, Antoine; Luyf, Angela; Koehler, Carla M; McCaffery, J Michael; Gottlieb, Eyal; Vaz, Frederic M; Claypool, Steven M.
Afiliación
  • Lu YW; Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185, USA.
  • Galbraith L; Cancer Research UK, The Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
  • Herndon JD; Department of Chemistry and Biochemistry, Molecular Biology Institute, and Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA 90095-1569, USA.
  • Lu YL; Division of Biology and Biomedical Sciences, Graduate School of Arts and Sciences, Washington University, St. Louis, MO 63130-4899, USA.
  • Pras-Raves M; Departments of Clinical Chemistry and Pediatrics, Laboratory Genetic Metabolic Diseases and.
  • Vervaart M; Departments of Clinical Chemistry and Pediatrics, Laboratory Genetic Metabolic Diseases and.
  • Van Kampen A; Bioinformatics Laboratory, Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Center, Amsterdam, The Netherlands and.
  • Luyf A; Bioinformatics Laboratory, Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Center, Amsterdam, The Netherlands and.
  • Koehler CM; Department of Chemistry and Biochemistry, Molecular Biology Institute, and Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA 90095-1569, USA.
  • McCaffery JM; Integrated Imaging Center, Department of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
  • Gottlieb E; Cancer Research UK, The Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
  • Vaz FM; Departments of Clinical Chemistry and Pediatrics, Laboratory Genetic Metabolic Diseases and.
  • Claypool SM; Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185, USA, sclaypo1@jhmi.edu.
Hum Mol Genet ; 25(9): 1754-70, 2016 05 01.
Article en En | MEDLINE | ID: mdl-26908608
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Piel / Factores de Transcripción / Mitocondrias Hepáticas / Síndrome de Barth / Fibroblastos / Mitocondrias Cardíacas / Mutación Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Piel / Factores de Transcripción / Mitocondrias Hepáticas / Síndrome de Barth / Fibroblastos / Mitocondrias Cardíacas / Mutación Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos