Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease-Reference-Cited by-同舟云学术

Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease

Published:2020-09-24 Issue:11 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Dong Kexian¹²,Liu Xiaogang³,Jia Xueyuan¹²,Miao Huanhuan⁴,Ji Wei¹²,Wu Jie¹²,Huang Yun¹²,Xu Lidan¹²,Zhang Xuelong¹²,Su Hui¹²,Ji Guohua¹²,Liu Peng¹²,Guan Rongwei¹²,Bai Jing¹²,Fu Songbin¹²^ORCID,Zhou Xianli⁴,Sun Wenjing¹²^ORCID

Affiliation:

1. Laboratory of Medical Genetics Harbin Medical University Harbin China

2. Key Laboratory of Preservation of Human Genetic Resources and Disease Control in China Ministry of Education Harbin Medical University Harbin China

3. Department of Nephrology The First Affiliated Hospital of Harbin Medical University Harbin China

4. In‐Patient Ultrasound Department The Second Affiliated Hospital of Harbin Medical University Harbin China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1467

Reference29 articles.

1. Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients

2. Bilateral cysts in the choroid plexus in a patient with autosomal dominant polycystic kidney disease

3. Autosomal dominant polycystic kidney disease

4. Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases

5. Identification of a pathogenic mutation in a Chinese pedigree with polycystic kidney disease;Dong K.;Molecular Medicine Reports,2019

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