The Indian Journal of Pediatrics

, Volume 84, Issue 6, pp 489–490 | Cite as

Novel NPHS1 Gene Mutations in two Chinese Infants with Congenital Nephrotic Syndrome

Scientific Letter


Nephrotic Syndrome Preterm Infant Full Term Infant Heterozygous Mutation Filter Barrier 
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    Guaragna MS, Cleto TL, Souza ML, et al. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: a novel mutation is described. Nephrology (Carlton). 2015; doi: 10.1111/nep.12667.Google Scholar
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Copyright information

© Dr. K C Chaudhuri Foundation 2017

Authors and Affiliations

  1. 1.Department of Pediatrics, Beijing Chaoyang HospitalCapital Medical UniversityBeijingChina

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