Genotype‐phenotype correlation and prognostic impact in Chinese patients with Alport Syndrome-Reference-Cited by-同舟云学术

Genotype‐phenotype correlation and prognostic impact in Chinese patients with Alport Syndrome

Published:2019-05-29 Issue:7 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Shang Shunlai¹^ORCID,Peng Fei¹²,Wang Tao¹^ORCID,Wu Xiaoyuan¹,Li Ping¹,Li Qinggang¹^ORCID,Chen Xiang M.¹

Affiliation:

1. Department of Nephrology, State Key Laboratory of Kidney Diseases, National Clinical Research Center for Kidney Diseases Chinese PLA General Hospital, Medical School of Chinese PLA, Chinese PLA Institute of Nephrology Beijing China

2. School of Medicine Nankai University Tianjin China

Funder

Beijing Nova Program

National Natural Science Foundation of China

General Hospital of People’s Liberation Army

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.741

Reference45 articles.

1. Genotype–Phenotype Correlation in X-Linked Alport Syndrome

2. Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis

3. Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis

4. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

5. Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome

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