Chinese Journal of Nephrology
Genotype and clinical phenotype analysis of autosomal recessive polycystic kidney disease caused by the novel compound heterozygous mutation of PKHD1 gene
Yang Junlan, Peng Siqi, Wei Zhiyuan, Wang Bin, Wang Fengmei, Wang Xiaobing, Zhang Xiaoliang
Chinese Journal of Nephrology . 2024, (6): 451 -457 .  DOI: 10.3760/cma.j.cn441217-20231016-01025

Copyright© by the Editorial Board of Chinese Journal of Nephrology, Chinese Medical Association and the First Affiliated Hospital of Sun Yat-sen University (Guangzhou) Journal Co., Ltd

Address: Floor 2, Longzhu building, No. 5, Zhusigang Second Road, Yuexiu District, Guangzhou (510080) Tel：(020)87331532　Email：cmaszb@mail.sysu.edu.cn

This system is designed and developed by Beijing magtec Technology Development Co., Ltd. with technical support: support@magtech.com.cn

粤ICP备10090623号