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.diegojavierfares.com/top-deal-Spitfire-Sapphires-90d-Skateboard-Wheels-58mm-p18591-great-pick/