Fig. 1From: A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case reportPedigree of Moroccan family with Joubert syndrome. Patients 1, 2 and 3 were 18-, 13- and 10-years old respectively. Their parents are first cousinsBack to article page