oculocutaneous albinismResearch
A recent analysis highlights a child with oculocutaneous albinism linked to compound heterozygous variants of the OCA2 gene. This study contributes to the understanding of genetic factors influencing this rare condition.
analysis of a child with oculocutaneous albinism due to compound heterozygous variants of oca2 gene
Original title: “[Analysis of a child with Oculocutaneous albinism due to compound heterozygous variants of OCA2 gene].”