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
A cryptic splicing mutation in the INF2 gene causing Charcot-Marie-Tooth disease with minimal glomerular dysfunction.
Echaniz-Laguna A et al.
Journal of the Peripheral Nervous System : Jpns, 2019
Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era.
Sampson MG et al.
Seminars in Nephrology, 2015
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