دورية أكاديمية
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.
| العنوان: | 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. |
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| المؤلفون: | BORK, K.1 (AUTHOR) bork@hautklinik.klinik.uni-mainz.de, WULFF, K.2 (AUTHOR), HARDT, J.3 (AUTHOR), WITZKE, G.1 (AUTHOR), LOHSE, P.4 (AUTHOR) |
| المصدر: | Haemophilia. Jul2014, Vol. 20 Issue 5, pe372-e375. 4p. 1 Diagram, 1 Graph. |
| قاعدة البيانات: | Academic Search Index |
| تدمد: | 13518216 |
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| DOI: | 10.1111/hae.12519 |