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Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations.
Brito, Sara; Thompson, Kyle; Campistol, Jaume; Colomer, Jaime; Hardy, Steven A; He, Langping; Fernández-Marmiesse, Ana; Palacios, Lourdes; Jou, Cristina; Jiménez-Mallebrera, Cecilia; Armstrong, Judith; Montero, Raquel; Artuch, Rafael; Tischner, Christin; Wenz, Tina; McFarland, Robert; Taylor, Robert W.
Afiliação
  • Brito S; Serviço de Pediatria, Centro Hospitalar de Leiria, Hospital de Santo André Leiria, Portugal ; Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain.
  • Thompson K; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
  • Campistol J; Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain.
  • Colomer J; Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain.
  • Hardy SA; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
  • He L; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
  • Fernández-Marmiesse A; Diagnosis and Treatment Unit for Inborn Errors of Metabolism, Hospital Clínico Universitario de Santiago de Compostela La Coruña, Spain.
  • Palacios L; Progenika Biopharma a Grifols Company Derio, Spain.
  • Jou C; Pathology Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
  • Jiménez-Mallebrera C; Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain.
  • Armstrong J; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical, Genetics and Rett Unit, Laboratory Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
  • Montero R; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
  • Artuch R; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
  • Tischner C; Cluster of Excellence, Cellular Stress Responses in Aging-Associated Diseases, Institute for Genetics, University of Cologne Cologne, Germany.
  • Wenz T; Cluster of Excellence, Cellular Stress Responses in Aging-Associated Diseases, Institute for Genetics, University of Cologne Cologne, Germany ; German Network for Mitochondrial Disorders Munich, Germany.
  • McFarland R; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
  • Taylor RW; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
Front Genet ; 6: 254, 2015.
Article em En | MEDLINE | ID: mdl-26284110
[This corrects the article on p. 102 in vol. 6, PMID: 25852744.].
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Genet Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Espanha
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Genet Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Espanha