Author:
Casaña Pilar,Martínez Francisco,Haya Saturnino,Espinós Carmen,Aznar José A.
Reference30 articles.
1. Practical application of three polymorphic microsatellites in intron 40 of the human von Willebrand factor gene;Casaña;Haemostasis,1995
2. Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: new mutations, R1315C and R1341W, associated with type 2M and 2B variants;Casaña;American Journal of Hematology,1998
3. Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene;Casaña;British Journal of Haematology,2000
4. Association of the 3467C→T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease;Casaña;Annals of Hematology,2001a
5. New mutations in the exon 28 of VWF gene detected in patients with different types of von Willebrand disease;Casaña;Haematologica,2001b
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32 articles.
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