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pro vyhledávání: '"Jonathon T. Wilde"'
Autor:
R. Campbell Tait, Will Lester, Jonathon T. Wilde, Derrick John Bowen, Frank Hill, Kate Khair, A. M. Cumming, K. John Pasi, Peter William Collins, Pamela Grundy, Paula H. B. Bolton-Maggs, Steven Keeney, David Keeling, Saad M. Enayat
Publikováno v:
British Journal of Haematology. 128:830-836
The molecular pathogenesis of type 1 von Willebrand disease (VWD) is uncertain in most patients. We examined 30 type 1 VWD families in the UK Haemophilia Centre Doctors' Organization study. Heterozygosity for Y/C1584 was present in eight of 30 (27%)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b0ce53ea386ad0e8235ea25ddec826b
https://doi.org/10.1111/j.1365-2141.2005.05375.x
https://doi.org/10.1111/j.1365-2141.2005.05375.x
