MST1R mutation as a genetic cause of Lady Windermere syndrome
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Publication year
2017Source
European Respiratory Journal, 49, 1, (2017), pp. 1601478, article 1601478ISSN
Publication type
Article / Letter to editor
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Organization
Internal Medicine
Human Genetics
Pathology
Medical Microbiology
Journal title
European Respiratory Journal
Volume
vol. 49
Issue
iss. 1
Page start
p. 1601478
Page end
p. 1601478
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: Metabolic Disorders 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; Human Genetics - Radboud University Medical Center; Internal Medicine - Radboud University Medical Center; Medical Microbiology - Radboud University Medical Center; Pathology - Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [243859]
- Electronic publications [130594]
- Faculty of Medical Sciences [92795]
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