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Article

Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.

European journal of haematology - 1 Mar 2007

Kunishima Shinji, Yoshinari Miyako, Nishio Hisanori, Ida Komei, Miura Takuma, Matsushita Tadashi, Hamaguchi Motohiro, Saito Hidehiko

Abstract excerpt

OBJECTIVE: MYH9 disorders are characterised by giant platelets, thrombocytopenia, and Döhle body-like cytoplasmic granulocyte inclusion bodies that result from mutations in MYH9, the gene for non-muscle myosin heavy chain-IIA (NMMHC-IIA). MYH9 R702 mutations are highly associated with Alport manifestations and result in Epstein syndrome. The aim of our study was to determine the haematological characteristics of...

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Source

Identifiers

PMID: 17241369
DOI: 10.1111/j.1600-0609.2006.00806.x

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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