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Acquired von Willebrand syndrome type 2A in a JAK2-positive essential thrombocythaemia-affected member of a large von Willebrand disease family with a novel autosomal dominant A1716P mutation

✍ Scribed by Giannini, S.; Solimando, M.; Fierro, T.; Baronciani, L.; Federici, A. B.; Gresele, P.


Book ID
120308447
Publisher
Schattauer
Year
2011
Tongue
English
Weight
200 KB
Volume
105
Category
Article
ISSN
0340-6245

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