Related Articles

• Identification of TYR mutations in patients with oculocutaneous albinism
• Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism
• Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing
• Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa
• Identification of a novel pathogenic mutation of the MYH3 gene in a family with distal arthrogryposis type 2B