Related Articles

• Identification of TCIRG1 and CLCN7 gene mutations in a patient with autosomal recessive osteopetrosis
• CLCN7 and TCIRG1 mutations in a single family: Evidence for digenic inheritance of osteopetrosis
• Identification of TYR mutations in patients with oculocutaneous albinism
• Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss
• Compound pathogenic mutation in the USH2A gene in Chinese RP families detected by whole‑exome sequencing