Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2
Jun-ke Xia,
Zhou-xian Bai,
Xue-chao Zhao,
Jing-jing Meng,
Chen Chen,
Xiang-dong Kong
Affiliations
Jun-ke Xia
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China
Zhou-xian Bai
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China
Xue-chao Zhao
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China
Jing-jing Meng
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China
Chen Chen
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China
Xiang-dong Kong
Corresponding author. Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, 1 Jianshe Road, Erqi District, Zhengzhou, 450052, China.; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China