Harnessing Transcriptomics to Decipher Dystonia Pathogenesis
Mov Disord
.
2022 May;37(5):891.
doi: 10.1002/mds.28980.
Epub 2022 Mar 12.
Authors
Avi Fellner
1
2
3
,
Kishore Raj Kumar
1
4
5
Affiliations
1
Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
2
Raphael Recanati Genetics Institute, Rabin Medical Center, Beilinson Hospital, Petah Tikva, Israel.
3
Department of Neurology, Rabin Medical Center, Beilinson Hospital, Petah Tikva, Israel.
4
Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, Concord, New South Wales, Australia.
5
Concord Clinical School, The University of Sydney, Concord, New South Wales, Australia.
PMID:
35277998
DOI:
10.1002/mds.28980
No abstract available
Publication types
Research Support, Non-U.S. Gov't
Comment
MeSH terms
Dystonia* / genetics
Dystonic Disorders* / complications
Dystonic Disorders* / genetics
Humans
Transcriptome / genetics