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Twenty-four novel hemophilia B mutations revealed by rapid scanning of the whole factor IX gene in a French population sample.
Ghanem, N; Costes, B; Martin, J; Vidaud, M; Rothschild, C; Foyer-Gazengel, C; Goossens, M.
Affiliation
  • Ghanem N; Laboratoire de Génétique Moléculaire, INSERM U91, Hôpital Henri-Mondor, Créteil, France.
Eur J Hum Genet ; 1(2): 144-55, 1993.
Article in En | MEDLINE | ID: mdl-8055323
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Collection: 01-internacional Database: MEDLINE Main subject: Factor IX / Hemophilia B / Mutation Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 1993 Type: Article Affiliation country: France
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Factor IX / Hemophilia B / Mutation Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 1993 Type: Article Affiliation country: France