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[Molybdenum cofactor deficiency caused by MOCS1 gene mutation: a case report].
Wu, Lian-Hong; Jiang, Yan; Hu, Yue.
Affiliation
  • Wu LH; Department of Neurology, Children's Hospital of Chongqing Medical University/National Clinical Research Center for Child Health and Disorders/Ministry of Education Key Laboratory of Child Development and Disorders/Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China.
  • Jiang Y; Department of Neurology, Children's Hospital of Chongqing Medical University/National Clinical Research Center for Child Health and Disorders/Ministry of Education Key Laboratory of Child Development and Disorders/Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China.
  • Hu Y; Department of Neurology, Children's Hospital of Chongqing Medical University/National Clinical Research Center for Child Health and Disorders/Ministry of Education Key Laboratory of Child Development and Disorders/Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China.
Zhongguo Dang Dai Er Ke Za Zhi ; 23(4): 416-419, 2021 Apr.
Article in Zh | MEDLINE | ID: mdl-33840416
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Full text: 1 Database: MEDLINE Main subject: Uric Acid / Metal Metabolism, Inborn Errors Limits: Humans / Male / Newborn Country/Region as subject: Asia Language: Zh Year: 2021 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Uric Acid / Metal Metabolism, Inborn Errors Limits: Humans / Male / Newborn Country/Region as subject: Asia Language: Zh Year: 2021 Type: Article