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Clinical Genetics of Prolidase Deficiency: An Updated Review.
Spodenkiewicz, Marta; Spodenkiewicz, Michel; Cleary, Maureen; Massier, Marie; Fitsialos, Giorgos; Cottin, Vincent; Jouret, Guillaume; Poirsier, Céline; Doco-Fenzy, Martine; Lèbre, Anne-Sophie.
Afiliación
  • Spodenkiewicz M; Service de génétique, AMH2, CHU Reims, UFR de médecine, 51100 Reims, France.
  • Spodenkiewicz M; SFR CAP SANTE, UFR de médecine, 51100 Reims, France.
  • Cleary M; CESM-Pôle de Santé Mentale, CRIA, CIC-EC 1410 CHU de La Réunion, 97448 Saint-Pierre CEDEX, La Réunion, France.
  • Massier M; Equipe MOODS Inserm U1178, CESP, 94807 Villejuif, France.
  • Fitsialos G; Great Ormond Street Hospital NHS Foundation Trust and NIHR Biomedical Research Centre, London WC1N 3JH, UK.
  • Cottin V; Service de génétique, AMH2, CHU Reims, UFR de médecine, 51100 Reims, France.
  • Jouret G; The European Center for Genetics and DNA Identification, DNAlogy. 98 Vouliagmenis Ave. Glyfada, 16674 Athens, Greece.
  • Poirsier C; Department of Respiratory Medicine, National Reference Coordinating Center for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, Lyon, France; Claude Bernard University, Lyon 1, UMR754, IVPC, F-69008 Lyon, France.
  • Doco-Fenzy M; National Center of Genetics-Laboratoire National de Santé, L-3555 Dudelange, Luxembourg.
  • Lèbre AS; Service de génétique, AMH2, CHU Reims, UFR de médecine, 51100 Reims, France.
Biology (Basel) ; 9(5)2020 May 21.
Article en En | MEDLINE | ID: mdl-32455636
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Biology (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Francia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Biology (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Francia