Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy
Publication year
2021Source
Molecular Genetics & Genomic Medicine, 9, 10, (2021), article e1797ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Gynaecology
Journal title
Molecular Genetics & Genomic Medicine
Volume
vol. 9
Issue
iss. 10
Subject
Radboudumc 0: Other Research RIHS: Radboud Institute for Health Sciences; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience; Gynaecology - Radboud University Medical Center; Human Genetics - Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [246423]
- Electronic publications [134025]
- Faculty of Medical Sciences [93307]
- Open Access publications [107550]
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