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Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation‐dependent probe amplification (MLPA)
Author(s) -
LEE S.T.,
KIM H.J.,
KIM D.K.,
SCHUIT R. J. L.,
KIM S.H.
Publication year - 2008
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/j.1538-7836.2008.02905.x
Subject(s) - multiplex ligation dependent probe amplification , antithrombin , genetics , mutation , antithrombin iii deficiency , thrombophilia , gene mutation , point mutation , medicine , gene duplication , gene , microbiology and biotechnology , biology , heparin , exon , pregnancy