Reply to: Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST
Mov Disord
.
2023 May;38(5):911-913.
doi: 10.1002/mds.29384.
Authors
Afshin Saffari
1
,
Darius Ebrahimi-Fakhari
1
Affiliation
1
Movement Disorders Program, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
PMID:
37303094
PMCID:
PMC11049670
DOI:
10.1002/mds.29384
No abstract available
Publication types
Letter
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Comment
MeSH terms
Humans
Spastic Paraplegia, Hereditary* / genetics
Spastin / genetics
Substances
SPAST protein, human
Spastin
Grants and funding
K08 NS123552/NS/NINDS NIH HHS/United States