A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy
Publication year
2017Source
Neuromuscular Disorders, 27, 11, (2017), pp. 1043-1046ISSN
Publication type
Article / Letter to editor
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Organization
Laboratory Medicine
Neurology
Paediatrics
Paediatrics - OUD tm 2017
Journal title
Neuromuscular Disorders
Volume
vol. 27
Issue
iss. 11
Page start
p. 1043
Page end
p. 1046
Subject
Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical Neuroscience; Radboudumc 3: Disorders of movement RIMLS: Radboud Institute for Molecular Life Sciences; Neurology - Radboud University Medical Center; Paediatrics - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [243399]
- Faculty of Medical Sciences [92493]
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