Related Articles

• Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa
• Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis
• PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population
• Identification of a novel mutation in CRYM in a Chinese family with hearing loss using whole‑exome sequencing
• Whole‑exome sequencing study identifies two novel rare variations associated with congenital talipes equinovarus