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Article

Double nucleotidic mutation of the MYH9 gene in a young patient with end-stage renal disease.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Jan 2004

Capria Maria, Andreucci Michele, Fuiano Laura, Mancuso Domenico, Cianfrone Paola, Comi Nicola, Mazza Giuseppe, Caglioti Alfredo, Fuiano Giorgio

Abstract excerpt

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Share to MYH9 gene
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Myosin Heavy Chains

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Source

Identifiers

PMID: 14671068
DOI: 10.1093/ndt/gfg475

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Double nucleotidic mutation of the MYH9 gene in a young patient with end-stage renal disease.PMID 14671068Read ↗

Description of a novel mutation leading to MYH9-related disease.Semantic proximity Read ↗

Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure: case report and review of the literature.Semantic proximity Read ↗

A case of MYH9 disorders caused by a novel mutation (p.K74E).Semantic proximity Read ↗

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.Semantic proximity Read ↗

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African AmericansSemantic proximity Read ↗

Apparent genotype-phenotype mismatch in a patient with MYH9-related disease: when the exception proves the rule.Semantic proximity Read ↗

Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 gene.Semantic proximity Read ↗

Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.Semantic proximity Read ↗

A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation.Semantic proximity Read ↗

Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.Semantic proximity Read ↗

Identification of the first in cis mutations in MYH9 disorder.Semantic proximity Read ↗

MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura.Semantic proximity Read ↗

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