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Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III.
Yubero, Dèlia; Montero, Raquel; O'Callaghan, Mar; Pineda, Mercè; Meavilla, Silvia; Delgadillo, Veronica; Sierra, Cristina; Altimira, Laura; Navas, Plácido; Pope, Simon; Oppenheim, Marcus; Neergheen, Viruna; Ghosh, Arunabha; Mills, Phillipa; Clayton, Peter; Footitt, Emma; Cleary, Maureen; Hargreaves, Iain; Jones, Simon A; Heales, Simon; Artuch, Rafael.
Afiliación
  • Yubero D; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Montero R; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • O'Callaghan M; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Pineda M; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Meavilla S; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Delgadillo V; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Sierra C; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Altimira L; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Navas P; Clinical Chemistry, Gastroenterology and Neurology Departments, Hospital Sant Joan de Déu, Barcelona, 08950, Spain.
  • Pope S; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Oppenheim M; Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide-CSIC-JA, Sevilla, Spain.
  • Neergheen V; Neurometabolic Unit, National Hospital, Queen Square, London, UK.
  • Ghosh A; Neurometabolic Unit, National Hospital, Queen Square, London, UK.
  • Mills P; Neurometabolic Unit, National Hospital, Queen Square, London, UK.
  • Clayton P; Willink Unit, Manchester Centre for Genomic Medicine, CMFT, University of Manchester, Manchester, UK.
  • Footitt E; Genetics and Genomic Medicine, UCL Institute of Child Health, London, UK.
  • Cleary M; Genetics and Genomic Medicine, UCL Institute of Child Health, London, UK.
  • Hargreaves I; Genetics and Genomic Medicine, UCL Institute of Child Health, London, UK.
  • Jones SA; Genetics and Genomic Medicine, UCL Institute of Child Health, London, UK.
  • Heales S; Neurometabolic Unit, National Hospital, Queen Square, London, UK.
  • Artuch R; Willink Unit, Manchester Centre for Genomic Medicine, CMFT, University of Manchester, Manchester, UK.
JIMD Rep ; 25: 1-7, 2016.
Article en En | MEDLINE | ID: mdl-26205433
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: JIMD Rep Año: 2016 Tipo del documento: Article País de afiliación: España
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: JIMD Rep Año: 2016 Tipo del documento: Article País de afiliación: España