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

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

The most common cause for severe cases of hemophilia A is the homologous recombination involving intron 22 and related sequences outside the F8 gene. F8 coding regions of the gene including the exon/intron junctions were sequenced in 10 Turkish hemophilia A patients all of whom have been typed negat...

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Bibliographic Details
Main Author: El Maarri, O. (author)
Other Authors: Berber, E. (author), Fidanci, I.D. (author), UN, C. (author), Aktuglu, G. (author), Gurgey, A. (author), Celkan, T. (author), Meral, A. (author), Oldenburg, J. (author), Graw, J. (author), Akar, N. (author), Caglayan, H. (author)
Format: article
Published: 2006
Online Access:http://hdl.handle.net/10725/6175
http://dx.doi.org/10.1111/j.1365-2516.2006.01302.x
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2516.2006.01302.x/full
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http://hdl.handle.net/10725/6175
http://dx.doi.org/10.1111/j.1365-2516.2006.01302.x
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2516.2006.01302.x/full

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