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Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory.
Salles, Juliette; Eddiry, Sanaa; Lacassagne, Emmanuelle; Laurier, Virginie; Molinas, Catherine; Bieth, Éric; Franchitto, Nicolas; Salles, Jean-Pierre; Tauber, Maithé.
Affiliation
  • Salles J; Université de Toulouse, Toulouse, France. Juliette.salles@hotmail.fr.
  • Eddiry S; Service de Psychiatrie et Psychologie, CHU de Toulouse, Toulouse, France. Juliette.salles@hotmail.fr.
  • Lacassagne E; Infinity (Toulouse Institute for Infectious and Inflammatory Diseases), INSERM UMR1291, CNRS UMR5051 , Université Paul Sabatier, Toulouse III, France. Juliette.salles@hotmail.fr.
  • Laurier V; Institut des Handicaps Neurologiques, Psychiatriques et Sensoriels, CHU de Toulouse, Toulouse, France. Juliette.salles@hotmail.fr.
  • Molinas C; Infinity (Toulouse Institute for Infectious and Inflammatory Diseases), INSERM UMR1291, CNRS UMR5051 , Université Paul Sabatier, Toulouse III, France.
  • Bieth É; Infinity (Toulouse Institute for Infectious and Inflammatory Diseases), INSERM UMR1291, CNRS UMR5051 , Université Paul Sabatier, Toulouse III, France.
  • Franchitto N; Centre de Référence Prader-Willi, Hôpital Marin, APHP, Hendaye, France.
  • Salles JP; Centre de Référence du Syndrome de Prader-Willi et Syndromes avec Troubles du Comportement Alimentaire, Unité D'endocrinologie, Obésités, Maladies Osseuses, Génétique et Gynécologie Médicale, Hôpital des Enfants, CHU Toulouse, Toulouse, France.
  • Tauber M; Service de Génétique Médicale, Hôpital Purpan, CHU, 31059, Toulouse, France.
Clin Epigenetics ; 13(1): 159, 2021 08 13.
Article in En | MEDLINE | ID: mdl-34389046
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / DNA Methylation / Neurodevelopmental Disorders / Nutrition Disorders Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Infant / Male Language: En Journal: Clin Epigenetics Year: 2021 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / DNA Methylation / Neurodevelopmental Disorders / Nutrition Disorders Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Infant / Male Language: En Journal: Clin Epigenetics Year: 2021 Document type: Article Affiliation country: