Your browser doesn't support javascript.
loading
Erratum to: Identification and Characterisation of a Novel Pathogenic Mutation in the Human Lipodystrophy Gene AGPAT2 : C48R: A Novel Mutation in AGPAT2.
Ramanathan, N; Ahmed, M; Raffan, E; Stewart, C L; O'Rahilly, S; Semple, R K; Raef, H; Rochford, J J.
Afiliación
  • Ramanathan N; University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0QQ, UK.
  • Ahmed M; Institute of Medical Biology, Immunos, 8A Biomedical Grove, 138648, Singapore, Republic of Singapore.
  • Raffan E; Department of Medicine, King Faisal Specialist Hospital and Research Centre, PO Box 3354, Riyadh, 11211, Saudi Arabia.
  • Stewart CL; University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0QQ, UK.
  • O'Rahilly S; Institute of Medical Biology, Immunos, 8A Biomedical Grove, 138648, Singapore, Republic of Singapore.
  • Semple RK; University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0QQ, UK.
  • Raef H; University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0QQ, UK.
  • Rochford JJ; Department of Medicine, King Faisal Specialist Hospital and Research Centre, PO Box 3354, Riyadh, 11211, Saudi Arabia.
JIMD Rep ; 9: E3, 2013.
Article en En | MEDLINE | ID: mdl-28597290

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: JIMD Rep Año: 2013 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: JIMD Rep Año: 2013 Tipo del documento: Article País de afiliación: Reino Unido