Fig. 6
From: Novel compound heterozygous mutations in LMAN2L cause early childhood refractory epilepsy

Sanger sequencing shows novel LMAN2L compound heterozygous variant inherited from the parents. c.476A>G (p.D159G) variant
From: Novel compound heterozygous mutations in LMAN2L cause early childhood refractory epilepsy
Sanger sequencing shows novel LMAN2L compound heterozygous variant inherited from the parents. c.476A>G (p.D159G) variant