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Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding.
Baronciani, L; Federici, A B; Beretta, M; Cozzi, G; Canciani, M T; Mannucci, P M.
Affiliation
  • Baronciani L; Angelo Bianchi Bonomi Haemophilia and Thrombosis Center, Department of Internal Medicine and Dermatology IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation and University of Milan, Milan, Italy. luciano.baronciani@unimi.it
J Thromb Haemost ; 3(12): 2689-94, 2005 Dec.
Article in En | MEDLINE | ID: mdl-16246252
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Collection: 01-internacional Database: MEDLINE Main subject: Von Willebrand Factor / Collagen / Mutation, Missense Limits: Adult / Animals / Female / Humans Country/Region as subject: Europa Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2005 Document type: Article Affiliation country: Italia Country of publication: Reino Unido
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Von Willebrand Factor / Collagen / Mutation, Missense Limits: Adult / Animals / Female / Humans Country/Region as subject: Europa Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2005 Document type: Article Affiliation country: Italia Country of publication: Reino Unido