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Article

Thrombin generation in two families with MYH9-related platelet disorder.

Platelets - 1 Jan 2016

Zetterberg Eva, Carlsson Alle Margareta S, Najm Juliane, Greinacher Andreas

Abstract excerpt

MYH9-related platelet disorders are inherited macrothrombocytopenias with additional clinical manifestations including renal failure, hearing loss, pre-senile cataract, and inclusion bodies in leucocytes that are present in different combinations. The MYH9 gene codes for the cytoplasmic contractile protein non-muscular myosin heavy chain IIA, present in several tissues. The bleeding tendency is usually mild to...

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Source

Identifiers

PMID: 26247237
DOI: 10.3109/09537104.2015.1064882

Genes

MYH9

Variants

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.

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