Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy

ConclusionThis deletion inKAT6B may affect protein function and cause corresponding clinical symptoms through interactions with key complexes and downstream products.

Source: Molecular Genetics & Genomic Medicine - June 9, 2023 Category: Genetics & Stem Cells Authors: Xiaoang Sun, Xiaona Luo, Longlong Lin, Simei Wang, Chunmei Wang, Fang Yuan, Xiaoping Lan, Jingbin Yan, Yucai Chen Tags: ORIGINAL ARTICLE Source Type: research