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Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.
Brunet, Theresa; Berutti, Riccardo; Dill, Veronika; Hecker, Judith S; Choukair, Daniela; Andres, Stephanie; Deschauer, Marcus; Diehl-Schmid, Janine; Krenn, Martin; Eckstein, Gertrud; Graf, Elisabeth; Gasser, Thomas; Strom, Tim M; Hoefele, Julia; Götze, Katharina S; Meitinger, Thomas; Wagner, Matias.
Affiliation
  • Brunet T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.
  • Berutti R; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.
  • Dill V; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.
  • Hecker JS; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.
  • Choukair D; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany.
  • Andres S; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany.
  • Deschauer M; Division of Paediatric Endocrinology and Diabetology, University Children's Hospital, 69120 Heidelberg, Germany.
  • Diehl-Schmid J; Center of Human Genetics and Laboratory Diagnostics, 82152 Martinsried, Germany.
  • Krenn M; Department of Neurology, Technical University of Munich, School of Medicine, 81675 Munich, Germany.
  • Eckstein G; Technical University of Munich, School of Medicine, Department of Psychiatry and Psychotherapy, 81675 Munich, Germany.
  • Graf E; Munich Cluster for Systems Neurology (SyNergy), 81377 Munich, Germany.
  • Gasser T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.
  • Strom TM; Department of Neurology, Medical University of Vienna, 1090 Vienna, Austria.
  • Hoefele J; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.
  • Götze KS; Core Facility Genomics, Helmholtz Center Munich, Neuherberg 85764, Germany.
  • Meitinger T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.
  • Wagner M; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, 72076 Tübingen, Germany.
Hum Mol Genet ; 31(14): 2386-2395, 2022 07 21.
Article de En | MEDLINE | ID: mdl-35179199

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Hématopoïèse clonale / Hématopoïèse Type d'étude: Observational_studies / Risk_factors_studies Limites: Aged / Humans Langue: En Journal: Hum Mol Genet Sujet du journal: BIOLOGIA MOLECULAR / GENETICA MEDICA Année: 2022 Type de document: Article Pays d'affiliation: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Hématopoïèse clonale / Hématopoïèse Type d'étude: Observational_studies / Risk_factors_studies Limites: Aged / Humans Langue: En Journal: Hum Mol Genet Sujet du journal: BIOLOGIA MOLECULAR / GENETICA MEDICA Année: 2022 Type de document: Article Pays d'affiliation: Allemagne