ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. (2016)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awv320
PubMed Identifier: 26556829
Publication URI: http://europepmc.org/abstract/MED/26556829
Type: Journal Article/Review
Volume: 139
Parent Publication: Brain : a journal of neurology
Issue: Pt 1
ISSN: 0006-8950