Identification of a pathogenic mutation in a Chinese pedigree with polycystic kidney disease-Reference-Cited by-同舟云学术

Identification of a pathogenic mutation in a Chinese pedigree with polycystic kidney disease

Published:2019-01-31 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Dong Kexian¹,Miao Huanhuan²,Jia Xueyuan¹,Wu Jie¹,Wu Han²,Sun Jiawei²,Ji Wei¹,Su Hui¹,Xu Lidan¹,Zhang Xuelong¹,Zhu Siqi¹,Ji Guohua¹,Guan Rongwei¹,Wang Hao³,Bai Jing¹,Yu Jingcui⁴,Sun Wenjing¹,Zhou Xianli²,Fu Songbin¹

Affiliation:

1. Laboratory of Medical Genetics, Harbin Medical University, Harbin, Heilongjiang 150081, P.R. China

2. In‑Patient Ultrasound Department, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150086, P.R. China

3. Department of Hepatopancreatobiliary Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150086, P.R. China

4. Scientific Research Centre, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150086, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

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2. Insights Into the Molecular Mechanisms of Polycystic Kidney Diseases;Frontiers in Physiology;2021-09-08

3. The heteromeric PC-1/PC-2 polycystin complex is activated by the PC-1 N-terminus;eLife;2020-11-09

4. Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease;Molecular Genetics & Genomic Medicine;2020-09-24