Clinical features and the genetic analysis of KAT6B-related diseases caused by a de novo mutation of the KAT6B gene c.621+1G>A

• Yu Yang,
• Hai-Meng Zhang,
• Hui Huang

Affiliations

Yu Yang

Corresponding author. Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, No. 122 Yangming Road, Donghu District, Nanchang 330006, Jiangxi, China.; Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, Nanchang, 330006, Jiangxi, China; Jiangxi Children's Genetic Metabolic Diseaseclinical Research Center, Nanchang, 330006, Jiangxi, China

Hai-Meng Zhang

Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, Nanchang, 330006, Jiangxi, China

Hui Huang

Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, Nanchang, 330006, Jiangxi, China