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Article

A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy

18 Jul 2017

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Share to Adenosine and Purinergic Signaling
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Share to Renal Diseases and Glomerulopathies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 28729035
DOI: 10.1016/j.kint.2017.04.025

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Related research

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A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathyPMID 28729035Read ↗

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CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.Semantic proximity Read ↗

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Clinical research advances of CFHR5 nephropathy: a recent review.Semantic proximity Read ↗

CFHR5 Genetic Variations and Serum Levels in Patients with Immune-Complex-Mediated Membranoproliferative Glomerulonephritis and C3-GlomerulopathySemantic proximity Read ↗

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