De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1186/s12959-016-0092-2.pdf
Reference21 articles.
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3. James PD, Lillicrap D. Von Willebrand disease: clinical and laboratory lessons learned from the large Von Willebrand disease studies. Am J Hematol. 2012;87 Suppl 1:S4–11.
4. Favaloro EJ. Diagnosis and classification of Von Willebrand disease: a review of the differential utility of various functional Von Willebrand factor assays. Blood Coagul Fibrinolysis. 2011;22:553–64.
5. Ahmad F, Oyen F, Jan R, Budde U, Schneppenheim R, Saxena R. Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in Von Willebrand disease. Haemophilia. 2014;20:e311–7.
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