RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy
Mov Disord
.
2020 Jul;35(7):1277-1279.
doi: 10.1002/mds.28074.
Epub 2020 Apr 24.
Authors
Roisin Sullivan
1
,
Wai Yan Yau
1
2
,
Viorica Chelban
1
2
,
Salvatore Rossi
1
,
E O'Connor
1
2
,
Nicholas W Wood
3
2
,
Andrea Cortese
1
4
,
Henry Houlden
1
2
Affiliations
1
Department of Neuromuscular Disease, Queen's Square Institute of Neurology, London, United Kingdom.
2
The National Hospital for Neurology and Neurosurgery, London, United Kingdom.
3
Movement Disorders, Queen's Square Institute of Neurology, London, United Kingdom.
4
Department of Brain and Behavioural Science, University of Pavia, Pavia, Italy.
PMID:
32333430
DOI:
10.1002/mds.28074
No abstract available
Publication types
Letter
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
MeSH terms
Atrophy
DNA Repeat Expansion
Humans
Introns / genetics
Multiple System Atrophy* / genetics
Grants and funding
WT104033/Z/14/Z/WT_/Wellcome Trust/United Kingdom
G0802760/MRC_/Medical Research Council/United Kingdom
U54 NS065712/NS/NINDS NIH HHS/United States
WT093205MA/WT_/Wellcome Trust/United Kingdom
MR/S01165X/1/MRC_/Medical Research Council/United Kingdom
MR/J004758/1/MRC_/Medical Research Council/United Kingdom
MR/T001712/1/MRC_/Medical Research Council/United Kingdom
G1001253/MRC_/Medical Research Council/United Kingdom
204841/Z/16/Z/WT_/Wellcome Trust/United Kingdom