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Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2.
Xia, Jun-Ke; Bai, Zhou-Xian; Zhao, Xue-Chao; Meng, Jing-Jing; Chen, Chen; Kong, Xiang-Dong.
Affiliation
  • Xia JK; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China. Electronic address: xiajunke1988@126.com.
  • Bai ZX; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China.
  • Zhao XC; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China.
  • Meng JJ; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China.
  • Chen C; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China.
  • Kong XD; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, China. Electronic address: kongxd@263.net.
Pediatr Neonatol ; 61(5): 558-560, 2020 10.
Article in En | MEDLINE | ID: mdl-32482602
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pediatr Neonatol Year: 2020 Document type: Article Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pediatr Neonatol Year: 2020 Document type: Article Country of publication: