PuSH - Publication Server of Helmholtz Zentrum München: Sequencing of the factor 8(F8)coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations and one rediagnosis of von Willebrand's disease type 2N.

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Berber, E.* ; Fidanci, I.D.* ; Un, C.* ; El-Maarri, O.* ; Aktuglu, G.* ; Gurgey, A.* ; Celkan, T.* ; Meral, A.* ; Oldenburg, J.* ; Graw, J. ; Akar, N.*

Sequencing of the factor 8(F8)coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations and one rediagnosis of von Willebrand's disease type 2N.

Haemophilia 12, 398-400 (2006)

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Open Access Green as soon as Postprint is submitted to ZB.

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Publication type Article: Journal article

Document type Scientific Article

Keywords DNA sequencing; factorVIII; haemophilia; mutation detection; rediagnosis; vWD 2N

ISSN (print) / ISBN 1351-8216

e-ISSN 1365-2516

Journal Haemophilia

Quellenangaben Volume: 12, Pages: 398-400

Publisher Wiley

Reviewing status Peer reviewed

Institute(s) Institute of Developmental Genetics (IDG)