Associated Papers
Novel Truncating Variants in PODXL Represent a New Entity to Be Explored Among Podocytopathies.
García-Aznar JM et al.
Genes, 2025
Atypical focal segmental glomerulosclerosis associated with a new PODXL nonsense variant.
Marx D et al.
Molecular Genetics & Genomic Medicine, 2021
The ATP Synthase Deficiency in Human Diseases.
Galber C et al.
Life (basel, Switzerland), 2021
Functional Genomics of PRUNE1 in Neurodevelopmental Disorders (NDDs) Tied to Medulloblastoma (MB) and Other Tumors.
Bibbò F et al.
Frontiers in Oncology, 2021
Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome.
Kang HG et al.
Experimental & Molecular Medicine, 2017
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