Fig. 3From: Clinical and genetic characteristics of Chinese patients with congenital cranial dysinnervation disordersGenomic sequence chromatograms of CFEOM individuals with KIF21A and TUBB3 variants. A Four heterozygous variants (R954W, R954Q, M947T and F355S) of KIF21A gene (red arrows). B Five heterozygous variants (S78T, R262C, R380C, E410K and R262H) of TUBB3 gene (red arrows)Back to article page