Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutation.
Identifieur interne : 000332 ( Main/Exploration ); précédent : 000331; suivant : 000333Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutation.
Auteurs : Mika H. Martikainen [Royaume-Uni] ; Grainne S. Gorman [Royaume-Uni] ; Paul Goldsmith [Royaume-Uni] ; David J. Burn [Royaume-Uni] ; Doug M. Turnbull [Royaume-Uni] ; Andrew M. Schaefer [Royaume-Uni]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
DOI: 10.1002/mds.26358
PubMed: 26265210
Affiliations:
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