Fig. 1From: A Japanese case of oculopharyngeal muscular dystrophy (OPMD) with PABPN1 c.35G > C; p.Gly12Ala point mutationPedigree of a Japanese family with oculopharyngeal muscular dystrophy with c.35G > C point mutation in the PABPN1 gene. Filled symbols indicate symptomatic at presentBack to article page