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Case Reports in Genetics
Volume 2017 (2017), Article ID 2357282, 7 pages
https://doi.org/10.1155/2017/2357282
Case Report

Three Novel Mutations in the NPHS1 Gene in Vietnamese Patients with Congenital Nephrotic Syndrome

1Institute of Genome Research, Vietnam Academy of Science and Technology, Hanoi, Vietnam
2Faculty of Medicine and Pharmacy, Vietnam National University, Hanoi, Vietnam
3Vietnam National Hospital of Pediatrics, Hanoi, Vietnam
4Hanoi Medical University, Hanoi, Vietnam

Correspondence should be addressed to Huy Hoang Nguyen

Received 8 November 2016; Revised 26 December 2016; Accepted 13 February 2017; Published 14 March 2017

Academic Editor: David B. Kershaw

Copyright © 2017 Thi Kim Lien Nguyen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Thi Kim Lien Nguyen, Van Dem Pham, Thu Huong Nguyen, Trung Kien Pham, Thi Quynh Huong Nguyen, and Huy Hoang Nguyen, “Three Novel Mutations in the NPHS1 Gene in Vietnamese Patients with Congenital Nephrotic Syndrome,” Case Reports in Genetics, vol. 2017, Article ID 2357282, 7 pages, 2017. doi:10.1155/2017/2357282