Familial association of genetic generalised epilepsy with limb-girdle muscular dystrophy through a mutation in CAPN3
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•We present a family that includes members with phenotypes of generalized epilepsy and limb-girdle muscular dystrophy.•Subjects with heterozygous mutation developed epilepsy; a subject with homozygous mutation developed limb-girdle dystrophy.•Mutations in C... ...
