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Article

Podocin mutations in a patient with congenital nephrotic syndrome and cardiac malformation.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Dec 2008

Sönmez Ferah, Mir Sevgi, Berdeli Afig, Aydoğdu Süleyman A, Altincik Ayça

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Share to Urinary Tract
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intracellular Signaling Peptides and Proteins

Share to Mutation, Missense

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Identifiers

PMID: 19067903
DOI: 10.1111/j.1442-200X.2008.02744.x

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Podocin mutations in a patient with congenital nephrotic syndrome and cardiac malformation.PMID 19067903Read ↗

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A missense mutation in podocin leads to early and severe renal disease in miceSemantic proximity Read ↗

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Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.Semantic proximity Read ↗

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