Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

• Jianlong Zhuang,
• Chunnuan Chen,
• Yuanbai Wang,
• Shuhong Zeng,
• Yu’e Chen,
• Yuying Jiang,
• Yingjun Xie,
• Yingjun Xie,
• Gaoxiong Wang

Affiliations

Jianlong Zhuang

Prenatal Diagnosis Center, Quanzhou Women’s and Children’s Hospital, Quanzhou, China

Chunnuan Chen

Department of Neurology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China

Yuanbai Wang

Prenatal Diagnosis Center, Quanzhou Women’s and Children’s Hospital, Quanzhou, China

Shuhong Zeng

Prenatal Diagnosis Center, Quanzhou Women’s and Children’s Hospital, Quanzhou, China

Yu’e Chen

Ultrasonography, Quanzhou Women’s and Children’s Hospital, Quanzhou, China

Yuying Jiang

Prenatal Diagnosis Center, Quanzhou Women’s and Children’s Hospital, Quanzhou, China

Yingjun Xie

Department of Obstetrics and Gynecology, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Yingjun Xie

Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Gaoxiong Wang

Quanzhou Women’s and Children’s Hospital, Quanzhou, China