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A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain
Author(s) -
KEELING D.,
BEAVIS J.,
MARR R.,
SUKHU K.,
BIGNELL P.
Publication year - 2012
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/j.1365-2516.2011.02676.x
Subject(s) - haemophilia , haemophilia b , medicine , thrombosis , haemophilia a , pediatrics
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