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Childhood onset dystonia, chorea or related movement disorder v6.8 EPM2A Arina Puzriakova Phenotypes for gene: EPM2A were changed from to Myoclonic epilepsy of Lafora 1, OMIM:254780
Childhood onset dystonia, chorea or related movement disorder v0.0 EPM2A Ellen McDonagh gene: EPM2A was added
gene: EPM2A was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red
Mode of inheritance for gene: EPM2A was set to