authors
- Tarnopolsky, Mark
- Brady, Lauren
- Tetreault, Martine
- Boycott, Kym
- MacKenzie, Alex
- Majewski, Jacek
- Brudno, Michael
- Bulman, Dennis
- Dyment, David
TRMT5
mutations are associated with features of complex hereditary spastic paraparesis
Journal Articles
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Overview
status
publication date
- November 21, 2017
has subject area
- 1103 Clinical Sciences (FoR)
- 1109 Neurosciences (FoR)
- 1702 Cognitive Sciences (FoR)
- Female (MeSH)
- Humans (MeSH)
- Middle Aged (MeSH)
- Neurology & Neurosurgery (Science Metrix)
- Paraparesis, Spastic (MeSH)
- Siblings (MeSH)
- Spastic Paraplegia, Hereditary (MeSH)
- tRNA Methyltransferases (MeSH)
published in
- Neurology Journal