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Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.
Quélin, Florence; Mathonnet, Florence; Potentini-Esnault, Catherine; Trigui, Nawel; Peynet, Jocelyne; Bastenaire, Brigitte; Guillon, Laurent; Bigel, Marie-Laure; Sauger, Annick; Mazurier, Claudine; de Mazancourt, Philippe.
Affiliation
  • Quélin F; Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Raymond Poincaré, Garches, France. Florence.quelin@rpc.ap-hop-paris.fr
Blood Coagul Fibrinolysis ; 17(1): 69-73, 2006 Jan.
Article in En | MEDLINE | ID: mdl-16607084
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Factor XI / Factor XI Deficiency / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2006 Document type: Article Affiliation country: Country of publication:
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Factor XI / Factor XI Deficiency / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2006 Document type: Article Affiliation country: Country of publication: