Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease.

Boczonadi, V; King, M S; Smith, A C; Olahova, M; Bansagi, B; Roos, A; Eyassu, F; Borchers, C; Ramesh, V; Lochmüller, H; Polvikoski, T; Whittaker, R G; Pyle, A; Griffin, H; Taylor, R W; Chinnery, P F; Robinson, A J; Kunji, E R S; Horvath, R

Boczonadi, V; King, M S; Smith, A C; Olahova, M; Bansagi, B; Roos, A; Eyassu, F; Borchers, C; Ramesh, V; Lochmüller, H; Polvikoski, T; Whittaker, R G; Pyle, A; Griffin, H; Taylor, R W; Chinnery, P F; Robinson, A J; Kunji, E R S; Horvath, R.

Afiliación

Boczonadi V; Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
King MS; Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Smith AC; Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Olahova M; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.
Bansagi B; Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
Roos A; Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
Eyassu F; Leibniz Institute of Analytic Sciences (ISAS), Dortmund, Germany.
Borchers C; Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Ramesh V; UVic-Genome BC Proteomics Centre, Vancouver, BC, Canada.
Lochmüller H; Department of Paediatric Neurology, Royal Victoria Infirmary, Newcastle upon Tyne Foundation Hospitals NHS Trust, Newcastle upon Tyne, UK.
Polvikoski T; Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
Whittaker RG; Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.
Pyle A; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.
Griffin H; Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
Taylor RW; Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
Chinnery PF; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.
Robinson AJ; Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Kunji ERS; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Horvath R; Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.

Genet Med ; 21(9): 2163-2164, 2019 Sep.

Article en En | MEDLINE | ID: mdl-31028354

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

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