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
All institutes and research themes of the Radboud University Medical Center; Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical Neuroscience; Radboudumc 3: Disorders of movement RIMLS: Radboud Institute for Molecular Life SciencesThis item appears in the following Collection(s)
- Academic publications [234316]
- Faculty of Medical Sciences [89180]
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