Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor

著录项

• 来源
  《Haemophilia: the official journal of the World Federation of Hemophilia》 |2014年第5期|共4页
• 作者

  Bork K.; Wulff K.; Hardt J.; Witzke G.; Lohse P.;

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• 作者单位

  Johannes Gutenberg Univ Mainz Dept Dermatol D-55131 Mainz Germany;

  Ernst Moritz Arndt Univ Greifswald Univ Med Greifswald Germany;

  Johannes Gutenberg Univ Mainz Dept Med Psychol &

  Med Sociol D-55131 Mainz Germany;

  Johannes Gutenberg Univ Mainz Dept Dermatol D-55131 Mainz Germany;

  Inst Lab Med &

  Human Genet Singen Germany;

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• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 妇产科学;
• 关键词

  coagulation factor XII; deletion; F12 gene; hereditary angioedema; mRNA analysis; normal C1 inhibitor;

  机译：凝血因子XII;缺失;F12基因;遗传性血管型;mRNA分析;正常C1抑制剂;