• Association between Variants in the <em>OCA2-HERC2</em> Region and Blue Eye Colour in <em>HERC2</em> rs12913832 AA and AG Individuals
• Black Piedra in an Amerindian Girl with Oculocutaneous Albinism Type 2
• Clinical and molecular genetic analysis of Angelman syndrome with oculocutaneous albinism type 2: A case report and literature review
• Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of Congo
• Complex interactions of Tyrp1 in the eye
• Concurrent PANK2 and OCA2 variants in a patient with retinal dystrophy, hypopigmented irides and neurodegeneration
• DeoxyArbutin and its derivatives inhibit tyrosinase activity and melanin synthesis without inducing reactive oxygen species or apoptosis
• Dermatologic manifestations in patients with the Hermansky-Pudlak syndrome types 1 and 3
• Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B
• Hermansky-Pudlak syndrome presenting with paranoid delusion
• Hermansky-Pudlak syndrome type 2: A rare cause of severe periodontitis in adolescents-A case study
• Hermansky-Pudlak Syndrome: Spectrum in Oman
• Heterochromia
• Identification and characterization of the compound heterozygous variants of TYR gene in a northern Chinese family with Oculocutaneous albinism type 1
• In silico screening and molecular dynamics simulation of disease-associated nsSNP in TYRP1 gene and its structural consequences in OCA3
• In vitro characterization of the intramelanosomal domain of human recombinant TYRP1 and its oculocutaneous albinism type 3-related mutant variants
• Low-vision intervention for oculocutaneous albinism in a Tertiary Eye Care Hospital in India
• Minimal Efficacy of Nitisinone Treatment in a Novel Mouse Model of Oculocutaneous Albinism, Type 3
• Mutant alleles at the brown locus encoding tyrosinase-related protein-1 (TRP-1) affect proliferation of mouse melanocytes in culture
• Ocular findings and a comparative study of hair, skin and iris color in Chinese patients with albinism
• Oculocutaneous albinism type 3 (OCA3): analysis of two novel mutations in TYRP1 gene in two Chinese patients
• Oculocutaneous albinism type 3: a Japanese girl with novel mutations in TYRP1 gene
• Regulation of tyrosinase processing and trafficking by organellar pH and by proteasome activity
• Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene
• Tyrp1 and oculocutaneous albinism type 3
• Tyrp1 Mutant Variants Associated with OCA3: Computational Characterization of Protein Stability and Ligand Binding