Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations.

Attali, O; Vinciguerra, C; Trzeciak, M C; Durin, A; Pernod, G; Gay, V; Ménart, C; Sobas, F; Dechavanne, M; Négrier, C

Attali, O; Vinciguerra, C; Trzeciak, M C; Durin, A; Pernod, G; Gay, V; Ménart, C; Sobas, F; Dechavanne, M; Négrier, C.

Affiliation

Attali O; Laboratoire d'Hémostase, Hôpital E. Herriot, INSERM U331, Lyon, France.

Thromb Haemost ; 82(5): 1437-42, 1999 Nov.

Article in En | MEDLINE | ID: mdl-10595634

Subject(s)

Factor IX/genetics; Hemophilia B/genetics; Mutation; Amino Acid Substitution; Blood Protein Electrophoresis; Codon/genetics; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Exons/genetics; Factor IX/chemistry; Frameshift Mutation; France; Gene Deletion; Genes; Genetic Testing; Heteroduplex Analysis; Humans; Point Mutation; Protein Structure, Tertiary; Sequence Analysis, DNA

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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: Thromb Haemost Year: 1999 Document type: Article

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