Novel Pathogenic Mutation of P209L in TRPC6 Gene Causes Adult Focal Segmental Glomerulosclerosis-Reference-Cited by-同舟云学术

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Novel Pathogenic Mutation of P209L in TRPC6 Gene Causes Adult Focal Segmental Glomerulosclerosis

Published:2024-02-05 Issue: Volume: Page:
ISSN:0006-2928
Container-title:Biochemical Genetics
language:en
Short-container-title:Biochem Genet

Author:

Yu Tianxi,Ji Yongqiang,Cui Xin,Liang Ning,Wu Shuang,Xiang Chongjun,Li Yue,Tao Huiying,Xie Yaqi,Zuo Hongwei,Wang Wenting,Khan Nauman,Ullah Kamran,Xu Fuyi,Zhang Yan,Lin Chunhua

Funder

Binzhou Medical University Research Start-up Fund

Taishan Scholar Program

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s10528-023-10651-y.pdf

Reference54 articles.

1. Ashbrook DG et al (2021) A platform for experimental precision medicine: the extended BXD mouse family. Cell Syst 12(3):235–247

2. Bahcall OG (2015) Genetic testing ACMG guides on the interpretation of sequence variants. Nat Rev Genet 16(5):256

3. Buscher AK et al (2010) Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol 5(11):2075–2084

4. Buscher AK et al (2012) Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients. Clin Nephrol 78(1):47–53

5. Caster DJ et al (2022) Efficacy and safety of immunosuppressive therapy in primary focal segmental glomerulosclerosis: a systematic review and meta-analysis. Kidney Med 4(8):100501

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