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Article

Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling

18 Sept 2018

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Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
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Share to Renal Diseases and Glomerulopathies

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30241959
DOI: 10.1053/j.ajkd.2018.06.034

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Related research

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Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic CounselingPMID 30241959Read ↗

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Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of MutationsSemantic proximity Read ↗

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Clinical genetic testing using a custom-designed steroid-resistant nephrotic syndrome gene panel: analysis and recommendations.Semantic proximity Read ↗

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Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membraneSemantic proximity Read ↗

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