Related Articles
Novel compound heterozygous mutations in <em>CYP1B1</em> identified in a Chinese family with developmental glaucoma
Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa
Steatocystoma multiplex is associated with the R94C mutation in the KRTl7 gene
Identification of a novel compound heterozygous <em>CYP4V2</em> variant in a patient with autosomal recessive retinitis pigmentosa
A genetic pedigree analysis to identify gene mutations involved in femoral head necrosis