De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-depent phenotyp, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.
Publication year
2000Source
American Journal of Human Genetics, 66, 1, (2000), pp. 26-35ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Cognitive Neuroscience
Neurology
Journal title
American Journal of Human Genetics
Volume
vol. 66
Issue
iss. 1
Page start
p. 26
Page end
p. 35
Subject
Neuromuscular and neurometabolic disorders; Neuromusculaire en neurometabole aandoeningenThis item appears in the following Collection(s)
- Academic publications [238441]
- Faculty of Medical Sciences [90373]
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