Autosomal dominant C1149R von Willebrand disease: Phenotypic findings and their implications

1. Pérez-Rodríguez, A.
2. García-Rivero, A.
3. Lourés, E.
4. López-Fernández, M.F.
5. Rodríguez-Trillo, A.
6. Batlle Fonrodona, F.J.

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DOI: 10.3324/HAEMATOL.2008.003301 GOOGLE SCHOLAR lock_openAcceso aberto editor

Fonte de datos: Scopus