A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findings. (2015)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.jns.2015.05.031
PubMed Identifier: 26049658
Publication URI: http://europepmc.org/abstract/MED/26049658
Type: Journal Article/Review
Volume: 355
Parent Publication: Journal of the neurological sciences
Issue: 1-2
ISSN: 0022-510X