Fig. 1From: A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavinThe genogram of this family and the variants of SLC52A2 c.1328G>A, p.Cys443Tyr, and c.1022_1023insC, Leu341Profs*103 in BVVLS proband and parentsBack to article page