Oculocutaneous albinism (OCA) is an inherited disorder affecting the visual system and skin pigmentation. Our aim was to evaluate genetic and clinical heterogeneity in a cohort of Slovenian paediatric patients with clinically suspected OCA using advanced molecular-genetics approach. In as much as 20 out of 25 patients. genetic variants explaining their clinical phenotype were identified. https://www.roneverhart.com/Brown-Paper-Luncheon-Napkin-Live-Joyfully-13-x-13-500-count-box/