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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
Author(s) -
Bork K.,
Wulff K.,
Hardt J.,
Witzke G.,
Lohse P.
Publication year - 2014
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.12519
Subject(s) - turkish , medicine , philosophy , classics , art , linguistics
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