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Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in

Jia Jiao1, Li Wang2, Fenfen Ni3

  • 1Department of Nephrology, 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 400015, PR China.

Genes & Diseases
|September 26, 2022
PubMed

Keywords:
Clinical phenotypesGenetic phenotypesMulticenter cohortNephrotic syndromePediatricWhole-exome sequencing

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