NARP mitochondriopathy: an unusual cause of progressive myoclonic epilepsy

Details

Serval ID
serval:BIB_41A9E8D520A5
Type
Article: article from journal or magazin.
Collection
Publications
Title
NARP mitochondriopathy: an unusual cause of progressive myoclonic epilepsy
Journal
Neurology
Author(s)
Jung J., Mauguiere F., Clerc-Renaud P., Ollagnon E., Mousson de Camaret B., Ryvlin P.
ISSN
1526-632X (Electronic)
ISSN-L
0028-3878
Publication state
Published
Issued date
2007
Volume
68
Number
17
Pages
1429-30
Language
english
Notes
Jung, J
Mauguiere, F
Clerc-Renaud, P
Ollagnon, E
Mousson de Camaret, B
Ryvlin, P
eng
Neurology. 2007 Apr 24;68(17):1429-30. doi: 10.1212/01.wnl.0000264019.53959.10.
Keywords
DNA, Mitochondrial/genetics, Electroencephalography, Electroretinography, Female, Gait Ataxia/etiology, Humans, Middle Aged, Mitochondrial Encephalomyopathies/classification/*complications/genetics, Mitochondrial Proton-Translocating ATPases/*genetics, Mutation, Missense, Myoclonic Epilepsies, Progressive/*genetics, Organ Specificity, Phenotype, Photic Stimulation, Point Mutation
Pubmed
Create date
29/11/2018 12:36
Last modification date
20/08/2019 13:42
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