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Platelet hyperreactivity explains the bleeding abnormality and macrothrombocytopenia in a murine model of sitosterolemia

Sitosterolemia is a rare, autosomal recessive disease caused by mutations in the adenosine triphosphate-binding cassette transporter genes ABCG5 or ABCG8 that result in accumulation of xenosterols in the body. Clinical manifestations include tendon xanthomas, premature coronary artery disease, hemol...

詳細記述

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書誌詳細
主要な著者: Kanaji, Taisuke, Kanaji, Sachiko, Montgomery, Robert R., Patel, Shailendra B., Newman, Peter J.
フォーマット: Artigo
言語:Inglês
出版事項: American Society of Hematology 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3795464/
https://ncbi.nlm.nih.gov/pubmed/23926302
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-06-510461
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