Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutation
Mov Disord
.
2015 Sep;30(10):1432-3.
doi: 10.1002/mds.26358.
Epub 2015 Aug 12.
Authors
Mika H Martikainen
1
,
Grainne S Gorman
1
,
Paul Goldsmith
2
,
David J Burn
2
,
Doug M Turnbull
1
,
Andrew M Schaefer
1
Affiliations
1
Wellcome Trust Center for Mitochondrial Research, United Kingdom, Newcastle University, Newcastle upon Tyne, United Kingdom.
2
Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, United Kingdom.
PMID:
26265210
PMCID:
PMC4737103
DOI:
10.1002/mds.26358
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Aged
DNA, Mitochondrial / genetics*
Humans
Male
Mutation
Myoclonic Cerebellar Dyssynergia / genetics*
Substances
DNA, Mitochondrial
Supplementary concepts
Hunt's syndrome
Grants and funding
096919/Wellcome Trust/United Kingdom
G0700718/MRC_/Medical Research Council/United Kingdom
MR/K000608/1/MRC_/Medical Research Council/United Kingdom