Varaico: Literature-Extracted Genetic Variants

Gene:INF2
Variant:p.C101R
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INF2

NM_022489.4:p.C101R

Associated Papers

Regulation of formin INF2 and its alteration in INF2-linked inherited disorders.

Labat-de-Hoz L et al.

Cellular and Molecular Life Sciences : Cmls, 2024

39586895 (PubMed )
Supplement: 18_2024_5499_MOESM3_ESM.xlsx › Table-S1

Exome-First Strategy in Adult Patients With CKD: A Cohort Study.

Doreille A et al.

Kidney International Reports, 2023

36938085 (PubMed )
Supplement: mmc3.xlsx › Sheet1

Role of formin INF2 in human diseases.

Zhao Y et al.

Molecular Biology Reports, 2022

The formin INF2 in disease: progress from 10 years of research.

Labat-de-Hoz L et al.

Cellular and Molecular Life Sciences : Cmls, 2020

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.

Nagano C et al.

Scientific Reports, 2020

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."