A novel frameshift mutation of COL4A5 in a Chinese family with presumed IgA nephropathy and chronic glomerulonephritis-Reference-Cited by-同舟云学术

A novel frameshift mutation of COL4A5 in a Chinese family with presumed IgA nephropathy and chronic glomerulonephritis

Published:2020-09-06 Issue:12 Volume:34 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Zhu Qian¹²,Zhou Cong¹²^ORCID,Wang Jing¹²^ORCID

Affiliation:

1. Department of Obstetrics and Gynecology West China Second University Hospital Sichuan University Chengdu China

2. Key Laboratory of Birth Defects and Related Diseases of Women and Children Ministry of Education Sichuan University Chengdu China

Funder

Department of Science and Technology of Sichuan Province

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23558

Reference21 articles.

1. Alport syndrome: its effects on the glomerular filtration barrier and implications for future treatment

2. Estimating prevalence in single-gene kidney diseases progressing to renal failure

3. Alport Syndrome: An Inherited Disorder of Renal, Ocular, and Cochlear Basement Membranes

4. Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

5. Preclinical Alterations in the Serum of COL(IV)A3–/– Mice as Early Biomarkers of Alport Syndrome

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: A Pathogenic Missense Variant of WT1 Cosegregates With Proteinuria in a Six-Generation Chinese Family With IgA Nephropathy;Frontiers in Medicine;2022-01-31