Year: 2009
Language: Japanese
Author(s): World Federation of Hemophilia
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Traditional Chinese
この患者向けハンドブックには、稀な凝固因子欠乏症の遺伝特性、診断、症状、管理についての基本情報が記載されています。
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of fibrinogen disorders, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia
Also Available In: Japanese This resource has also been translated into the following languages, with permission from the WFH, by
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