Journal article
TRMT5 mutations are associated with features of complex hereditary spastic paraparesis
Authors
Tarnopolsky MA; Brady L; Tetreault M; Boycott K; MacKenzie A; Majewski J; Brudno M; Bulman D; Dyment D
Journal
Neurology, Vol. 89, No. 21, pp. 2210–2211
Publisher
Wolters Kluwer
Publication Date
November 21, 2017
DOI
10.1212/wnl.0000000000004657
ISSN
0028-3878