Monoallelic pathogenic <i>IFT140</i> variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotype.

Authors:
Dordoni C; Zeni L; Toso D; Mazza C; Mescia F and 6 more

Journal:
Clin Kidney J

Publication Year: 2024

DOI:
10.1093/ckj/sfae026

PMCID:
PMC10894029

PMID:
38404363

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Journal Information

Journal Title: Clin Kidney J

Detailed journal information not available.

Publication Details

Subject Category: Urology & Nephrology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
3/6
50.0% Transparent
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Evidence found in paper:

"CONFLICT OF INTEREST STATEMENT F.A. has received consulting fees from GSK, Vifor Pharma, AstraZeneca and Novartis. All other authors have declared no conflicts of interest."

Evidence found in paper:

"FUNDING None declared."

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Open Access
Paper is freely available to read
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Tool: rtransparent

OST Version: N/A

Last Updated: Aug 05, 2025