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[Advances in the diagnosis and treatment of phosphomannomutase 2 deficiency]

Shu-Yan Zhou1

  • 1Department of Gastroenterology, 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 = Chinese Journal of Contemporary Pediatrics
|February 28, 2023
PubMed

Keywords:
Congenital disorder of glycosylationGene mutationPMM2 genePhosphomannomutase 2 deficiency

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