Figure 1From: Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathiesPie charts summarizing mutation analysis in MKS and MKS-like patients. a) frequency of genes mutated in MKS and MKS-like phenotype; b) frequency of MKS genes mutations in consanguineous patients; c) common mutations in MKS1; d) common mutations in TMEM67; e) frequency of MKS genes mutations in non-consanguineous patients.Back to article page