Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleProgressive myoclonic epilepsy due to lafora body disease with a novel mutation.AuthorsIsrani, Anil; Mandal, AnirbanSubjectsDIAGNOSIS of epilepsy; GENETICS of epilepsy; ATROPHY; BRAIN; ELECTROENCEPHALOGRAPHY; ENZYMES; EPILEPSY; MAGNETIC resonance imaging; INBORN errors of metabolism; MITOCHONDRIAL pathology; GENETIC mutation; NEURONAL ceroid-lipofuscinosis; GENETIC testing; SEQUENCE analysis; DIAGNOSISPublicationJournal of Pediatric Neurosciences, 2018, Vol 13, Issue 1, p123ISSN1817-1745Publication typeArticleDOI10.4103/JPN.JPN_13_17