Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases.
Publication year
2000Source
Human Genetics, 106, (2000), pp. 432-439ISSN
Publication type
Article / Letter to editor
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Organization
Neurology
Otorhinolaryngology
Journal title
Human Genetics
Volume
vol. 106
Page start
p. 432
Page end
p. 439
Subject
Genetical and metabolic aspects of neuromuscular diseases; Clinical description and delineation of genetic syndromes; Genetische en metabole aspecten van neuromusculaire aandoeningen; Klinische beschrijving en moleculaire definiëring van genetische syndromenThis item appears in the following Collection(s)
- Academic publications [243984]
- Faculty of Medical Sciences [92811]
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