Fig. 3From: First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 genea Variation c.966C > A (p.Y322*) at homozygous state in the exon 10 of ERCC8 gene in patient A. b Variation c.2008C > T (p.R670W) in ERCC6 gene in family B: (i)Father, (ii)Mother and (iii)Patient B. c The novel variation c.843 + 1G > C in the junction exon9-intron9 of ERCC8 gene in patient CBack to article page