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Article

Advances in the understanding of MYH9 disorders.

Current opinion in hematology - 1 Sept 2010

Kunishima Shinji, Saito Hidehiko

Abstract excerpt

PURPOSE OF REVIEW: MYH9 disorders are autosomal dominant macrothrombocytopenias with leukocyte inclusion bodies caused by mutations in MYH9, the gene for the nonmuscle myosin heavy chain IIA. May-Hegglin anomaly and Sebastian, Fechtner, and Epstein syndromes belong to MYH9 disorders. The present...

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Source

Identifiers

PMID: 20601875
DOI: 10.1097/MOH.0b013e32833c069c

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20601875-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Advances in the understanding of MYH9 disorders.PMID 20601875Read ↗

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

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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 ↗

Linking the Landscape of MYH9-Related Diseases to the Molecular Mechanisms that Control Non-Muscle Myosin II-A Function in Cells.Semantic proximity Read ↗

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.Semantic proximity Read ↗

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias.Semantic proximity Read ↗

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Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?Semantic proximity Read ↗

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