Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report.

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🔗 View Article (PMID 27004562)

Published in BMC Pediatr on March 22, 2016

Authors

Liru Qiu1, Jianhua Zhou2

Author Affiliations

1: Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, 430030, China.
2: Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, 430030, China. jhzhou@tjh.tjmu.edu.cn.

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