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Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort.
- Source :
-
Haematologica [Haematologica] 2010 Dec; Vol. 95 (12), pp. 2163-5. Date of Electronic Publication: 2010 Sep 17. - Publication Year :
- 2010
Details
- Language :
- English
- ISSN :
- 1592-8721
- Volume :
- 95
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Haematologica
- Publication Type :
- Report
- Accession number :
- 20851871
- Full Text :
- https://doi.org/10.3324/haematol.2010.027177