Identifying gene mutations of Chinese patients with polycystic kidney disease through targeted next‐generation sequencing technology
Abstract Background Polycystic kidney disease (PKD) is the most common hereditary kidney disease. The main mutational genes causing autosomal dominant polycystic kidney disease (ADPKD) are PKD1 and PKD2 as well as some rare pathogenic genes. Unilateral PKD is rare in clinics, and its association wit...
Main Authors: | Tao Wang, Qinggang Li, Shunlai Shang, Guangrui Geng, Yuansheng Xie, Guangyan Cai, Xiangmei Chen |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2019-06-01
|
Series: | Molecular Genetics & Genomic Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/mgg3.720 |
Similar Items
-
A single-center analysis of genotype–phenotype characteristics of Chinese patients with autosomal dominant polycystic kidney disease by targeted exome sequencing
by: Ziyan Yan, et al.
Published: (2022-09-01) -
Identification of Three Novel Frameshift Mutations in the PKD1 Gene in Iranian Families with Autosomal Dominant Polycystic Kidney Disease Using Efficient Targeted Next-Generation Sequencing
by: Fariba Ranjzad, et al.
Published: (2018-03-01) -
Novel method for the genomic analysis of PKD1 mutation in autosomal dominant polycystic kidney disease
by: Shunlai Shang, et al.
Published: (2023-01-01) -
Novel Mutations in the PKD1 and PKD2 Genes of Chinese Patients with Autosomal Dominant Polycystic Kidney Disease
by: Dechao Xu, et al.
Published: (2018-03-01) -
Gene Panel Analysis in a Large Cohort of Patients With Autosomal Dominant Polycystic Kidney Disease Allows the Identification of 80 Potentially Causative Novel Variants and the Characterization of a Complex Genetic Architecture in a Subset of Families
by: Vilma Mantovani, et al.
Published: (2020-05-01)