Work

The E1841K Mutation in MYH-9 of a Patient with May-Hegglin Anomaly Inhibits the Disassembly of Non-Muscle Myosin IIA (MYH-9) Responsible for the Phenotype of the Disease.

Year: 2004

Type: article

Source: Blood

DOI: 10.1182/blood.v104.11.736.736

Authors: Koji Miyazaki, Satoshi Komatsu, Mariko Watanabe, Naoya Nakadate, Mitsuo Ikebe, Masaaki Higashihara

Institutions: Kitasato University, University of Massachusetts Chan Medical School

Language: English

Topic: Platelet Disorders and Treatments

Subfield: Hematology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2579183696

FWCI: 0.212

Cites:

Cited by: 1

Related to: 10