Author:
Dibbens L.M.,Michelucci R.,Gambardella A.,Andermann F.,Rubboli G.,Bayly M.A.,Joensuu T.,Vears D.F.,Franceschetti S.,Canafoglia L.,Wallace R.,Bassuk A.G.,Power D.A.,Tassinari C.A.,Andermann E.,Lehesjoki A.E.,Berkovic S.F.
Subject
Neurology (clinical),Neurology
Reference14 articles.
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3. A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome;Bassuk;Am J Hum Genet,2008
4. Unverricht-Lundborg phenotype not linked to EPM1 gene in Italian families: genetic heterogeneity or new disease entities?;Tassinari;Epilepsia,1996
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