Article

Lack of the human choline transporter-like protein CTL2 causes hearing impairment and a rare red blood cell phenotype

2022-05-16

Abstract excerpt

Recent genome-wide association and murine studies identified the human neutrophil antigen -3a/b polymorphism (HNA-3a/b) in SLC44A2 (rs2288904-G/A) as a risk factor in venous thromboembolism (VTE). The choline transporter-like protein CTL2 encoded by the SLC44A2 gene plays an important role in platelet aggregation and neutrophil interaction with the von Willebrand factor. By investigating alloantibodies to a high-p...

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Literature Corpus work: 791f1fd0-200a-590f-b7da-794c51dbb50f
DOI: 10.1101/2022.05.13.22273920

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