Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes. (2017)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00415-016-8312-z
PubMed Identifier: 27785568
Publication URI: http://europepmc.org/abstract/MED/27785568
Type: Journal Article/Review
Volume: 264
Parent Publication: Journal of neurology
Issue: 1
ISSN: 0340-5354