Open AccessReply: Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what’s in a name?
Author(s) -
Rebecca Schüle
Publication year - 2017
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awx282
Subject(s) - hereditary spastic paraplegia , spastic , mutation , paraplegia , medicine , genetics , leukodystrophy , physical medicine and rehabilitation , biology , psychiatry , phenotype , gene , cerebral palsy , spinal cord , disease
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