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Title: MST1R mutation as a genetic cause of Lady Windermere syndrome
Author(s): Becker, K.L. ; Arts, P.; Jaeger, M.; Plantinga, T.S. ; Gilissen, C.F. ; Laarhoven, A. van; Ingen, J. van ; Veltman, J.A. ; Joosten, L.A.B. ; Hoischen, A. ; Netea, M.G. ; Iseman, M.D.; Chan, E.D.; Veerdonk, F.L. van de
Publication year: 2017
Source: European Respiratory Journal, vol. 49, iss. 1, (2017), article 1601478
ISSN: 0903-1936
DOI: https://doi.org/10.1183/13993003.01478-2016
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/169740   https://hdl.handle.net/2066/169740

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Subject: Radboudumc 4: lnfectious Diseases and Global Health RIHS: Radboud Institute for Health Sciences
Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life Sciences
Radboudumc 6: Mitochondrial diseases RIMLS: Radboud Institute for Molecular Life Sciences
Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience
Radboudumc 9: Rare cancers RIMLS: Radboud Institute for Molecular Life Sciences
Organization: Internal Medicine
Human Genetics
Pathology
Medical Microbiology
Journal title:
European Respiratory Journal
Volume: vol. 49
Issue: iss. 1
Article number: 1601478

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