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.parisnaturalfoodes.shop/product-category/76-maca-choc-bar/
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