Open AccessSpg3a Mutation Co-Segregates with Hereditary Spastic Paraplegia Phenotype Whereas SPG31 Duplication Does Not
Author(s) -
Shera Gustafsson,
Thomas Sejersen
Publication year - 2012
Publication title -
journal of neurology and neurophysiology
Language(s) - English
Resource type - Journals
ISSN - 2155-9562
DOI - 10.4172/2155-9562.1000129
Subject(s) - hereditary spastic paraplegia , phenotype , gene duplication , paraplegia , mutation , spastic , genetics , neuroscience , medicine , bioinformatics , biology , gene , physical medicine and rehabilitation , spinal cord , cerebral palsy
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