DCT

Publications

Pennamen P et al. Dopachrome tautomerase variants in patients with oculocutaneous albinism. Genet. Med. 23: 479-487, 2021. PMID: 33100333.

Volk AE et al. Biallelic mutations in L-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism. Hum. Genet. 140: 1157-1168, 2021. PMID: 33959807.

Tingaud-Sequeira A et al. The Dct-/- Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism. Genes (Basel). 2022;13(7):1164. doi: 10.3390/genes13071164. PMID: 35885947; PMCID: PMC9324463.