Fig. 2From: Acute recurrent rhabdomyolysis in a Chinese boy associated with a novel compound heterozygous LPIN1 variant: a case reportDirect sequencing showing two alleles of the proband and his parents, respectively. The proband is a compound heterozygote of c.2047A > G and p.Q703delin sQE. The first variant is from the father, and the latter is from the mother. The arrow shows the variant point. P proband, F father, M mother, WT wild typeBack to article page