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Article

MYH9 gene mutations associated with bleeding.

Platelets - 1 May 2017

Savoia Anna, De Rocco Daniela, Pecci Alessandro

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28368695
DOI: 10.1080/09537104.2017.1294250

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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MYH9 gene mutations associated with bleeding.PMID 28368695Read ↗

[Analysis of clinical phenotype and gene mutation characteristics of MYH9-related disorder].Semantic proximity Read ↗

Giant platelet syndromes and the MYH9 mutations.Semantic proximity Read ↗

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

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

A novel MYH9 variant in a Chinese patient with MYH9 related diseaseSemantic proximity Read ↗

A case report of a family with MYH9 gene mutation-related disease in an ethnic minority group and literature review.Semantic proximity Read ↗

A Trp33Arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin anomaly.Semantic proximity Read ↗

MYH-9 Related Platelet Disorders: Strategies for Management and DiagnosisSemantic proximity Read ↗

Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias.Semantic proximity Read ↗

[Molecular diagnosis of a family with May-Hegglin anomaly].Semantic proximity Read ↗

A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan.Semantic proximity Read ↗

A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities.Semantic proximity Read ↗

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