Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM

Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM

<p>Abstract</p> <p>Background</p> <p>Hemophilia A represents the most common and severe inherited hemorrhagic disorder. It is caused by mutations in the F8 gene, which leads to a deficiency or dysfunctional factor VIII protein, an essential cofactor in the factor X acti...

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Main Authors: Chang Chieh-Ting (Author), Chiou Shyh-Shin (Author), Tsay Woei (Author), Hung Chia-Cheng (Author), Su Yi-Ning (Author), Lin Shin-Yu (Author), Ho Hong-Nerng (Author), Lee Chien-Nan (Author)
Format: Book
Published: BMC, 2008-06-01T00:00:00Z.
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