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Early onset or syndromic epilepsy v1.191 | MEF2C | Rebecca Foulger Source Wessex and West Midlands GLH was added to MEF2C. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy v1.190 | MEF2C | Rebecca Foulger Source NHS GMS was added to MEF2C. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy v1.189 | MEF2C | Rebecca Foulger reviewed gene: MEF2C: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy v1.188 | MEF2C | Tracy Lester reviewed gene: MEF2C: Rating: GREEN; Mode of pathogenicity: ; Publications: 20513142; Phenotypes: chromosome 5q14.3 deletion syndrome,613443, Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations,613443; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy | MEF2C | Sarah Leigh Added gene to panel |