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Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX.
Row, Céline; Chamouni, Pierre; Berger, Claire; Lienhart, Anne; Meunier, Sandrine; Fretigny, Mathilde; Dalibard, Vincent; Viprey, Marie; Chambost, Hervé; Barbay, Virginie; Bovet, Julien.
Afiliação
  • Row C; Thrombosis and Hemostasis Unit, University Hospital of Dijon, Dijon, France.
  • Chamouni P; Hemophilia Treatment Center, University Hospital of Rouen, Rouen, France.
  • Berger C; Hemophilia Treatment Center, Pediatric Hematology department, University Hospital of Saint Etienne, Saint Etienne, France.
  • Lienhart A; Hospices Civils de Lyon, French Reference Centre for Hemophilia, University Hospital of Lyon, France.
  • Meunier S; Hospices Civils de Lyon, French Reference Centre for Hemophilia, University Hospital of Lyon, France.
  • Fretigny M; Hemostasis Laboratory, University Hospital of Lyon, Lyon, France.
  • Dalibard V; Lille CHRU, Hemophilia Treatment Center, Hematology and Transfusion, Lille, France.
  • Viprey M; APHM, FranceCoag, Research Department, Marseille, France.
  • Chambost H; APHM, FranceCoag, Research Department, Marseille, France.
  • Barbay V; Aix-Marseille Univ, EA 3279 CEReSS-Health Service Research and Quality of Life Center, Marseille, France.
  • Bovet J; APHM, Hemophilia Treatment Center, La Timone Hospital and Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.
Haemophilia ; 27(4): e462-e465, 2021 Jul.
Article em En | MEDLINE | ID: mdl-32996663
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemofilia B / Hemofilia A Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemofilia B / Hemofilia A Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article