A RARE GENETIC DISORDER CAUSED BY A KAT6B MUTATION: PHENOTYPIC MANIFESTATIONS BASED ON A CLINICAL CASE

Authors	Tokarchuk N., Chekotun T., Starynets L.
Journal	Neonatology, Surgery and Perinatal Medicine
Publication Date	2025-12-29
DOI	10.24061/2413-4260.xv.4.58.2025.32