Open AccessA clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia
Author(s) -
P.A. Wilkinson
Publication year - 2004
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/awh299
Subject(s) - hereditary spastic paraplegia , medicine , paraplegia , genetics , mutation , spastic , physical medicine and rehabilitation , biology , gene , phenotype , psychiatry , spinal cord , cerebral palsy
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