Case Report: Genetic analysis of oculocutaneous albinism type 2 caused by a new mutation in the OCA2
Front Pediatr. 2025 Apr 17;13:1508198. doi: 10.3389/fped.2025.1508198. eCollection 2025. ABSTRACT Oculocutaneous albinism (OCA) is a condition inherited in an autosomal recessive manner, leading to reduced …