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Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway.
Ziosi, Marcello; Di Meo, Ivano; Kleiner, Giulio; Gao, Xing-Huang; Barca, Emanuele; Sanchez-Quintero, Maria J; Tadesse, Saba; Jiang, Hongfeng; Qiao, Changhong; Rodenburg, Richard J; Scalais, Emmanuel; Schuelke, Markus; Willard, Belinda; Hatzoglou, Maria; Tiranti, Valeria; Quinzii, Catarina M.
Afiliación
  • Ziosi M; Department of Neurology, Columbia University Medical Center, New York, NY, USA.
  • Di Meo I; Unit of Molecular Neurogenetics, IRCCS Foundation Neurological Institute "Carlo Besta", Milan, Italy.
  • Kleiner G; Department of Neurology, Columbia University Medical Center, New York, NY, USA.
  • Gao XH; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, USA.
  • Barca E; Department of Neurology, Columbia University Medical Center, New York, NY, USA.
  • Sanchez-Quintero MJ; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
  • Tadesse S; Department of Neurology, Columbia University Medical Center, New York, NY, USA.
  • Jiang H; Department of Neurology, Columbia University Medical Center, New York, NY, USA.
  • Qiao C; Irving Institute for Clinical and Translational Research, Columbia University Medical Center, New York, NY, USA.
  • Rodenburg RJ; Irving Institute for Clinical and Translational Research, Columbia University Medical Center, New York, NY, USA.
  • Scalais E; Department of Pediatrics, Radboud Center for Mitochondrial Medicine (RCMM), RadboudUMC, Nijmegen, The Netherlands.
  • Schuelke M; Division of Paediatric Neurology, Department of Paediatrics, Centre Hospitalier de Luxembourg, Luxembourg City, Luxembourg.
  • Willard B; Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Hatzoglou M; Mass Spectrometry Laboratory for Protein Sequencing, Learner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Tiranti V; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, USA.
  • Quinzii CM; Unit of Molecular Neurogenetics, IRCCS Foundation Neurological Institute "Carlo Besta", Milan, Italy valeria.tiranti@istituto-besta.it cmq2101@cumc.columbia.edu.
EMBO Mol Med ; 9(1): 96-111, 2017 01.
Article en En | MEDLINE | ID: mdl-27856618
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ataxia / Sulfuros / Ubiquinona / Debilidad Muscular / Enfermedades Mitocondriales Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: EMBO Mol Med Asunto de la revista: BIOLOGIA MOLECULAR Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ataxia / Sulfuros / Ubiquinona / Debilidad Muscular / Enfermedades Mitocondriales Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: EMBO Mol Med Asunto de la revista: BIOLOGIA MOLECULAR Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos