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Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
JAMA Neurol. 2016 Sep 1;73(9):1105-14. doi: 10.1001/jamaneurol.2016.2215.
JAMA Neurol. 2016.
PMID: 27400454
Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg disease.
Berrechid AG, Bendjebara M, Bouteiller D, Nasri A, Peuvion JN, Marie Y, Baulac S, Mrabet S, Ribierre T, Cazeneuve C, Imenkacem, Leguern E, Gouider R.
Berrechid AG, et al. Among authors: peuvion jn.
Epileptic Disord. 2019 Aug 1;21(4):359-365. doi: 10.1684/epd.2019.1078.
Epileptic Disord. 2019.
PMID: 31368437
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