Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.
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| Title: | Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. |
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| Authors: | Brunet T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany., Berutti R; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany., Dill V; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany., Hecker JS; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany., Choukair D; Division of Paediatric Endocrinology and Diabetology, University Children's Hospital, 69120 Heidelberg, Germany., Andres S; Center of Human Genetics and Laboratory Diagnostics, 82152 Martinsried, Germany., Deschauer M; Department of Neurology, Technical University of Munich, School of Medicine, 81675 Munich, Germany., Diehl-Schmid J; Technical University of Munich, School of Medicine, Department of Psychiatry and Psychotherapy, 81675 Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), 81377 Munich, Germany., Krenn M; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Department of Neurology, Medical University of Vienna, 1090 Vienna, Austria., Eckstein G; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.; Core Facility Genomics, Helmholtz Center Munich, Neuherberg 85764, Germany., Graf E; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Gasser T; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, 72076 Tübingen, Germany.; German Center for Neurodegenerative Diseases (DZNE), 72076 Tübingen, Germany., Strom TM; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Hoefele J; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Götze KS; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany., Meitinger T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Wagner M; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany. |
| Source: | Human molecular genetics [Hum Mol Genet] 2022 Jul 21; Vol. 31 (14), pp. 2386-2395. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1460-2083 |
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| DOI: | 10.1093/hmg/ddac034 |
