Published in Blood Weekly, October 19th, 2006
Study 1: According to recently published research from Canada, DNA microarray analysis detects mutations in hemophilia A.
"Congenital deficiency of factor (F) VIII results in the inherited X-linked bleeding disorder hemophilia A. More than 900 different mutations are reported in the hemophilia A mutation database with the largest number of mutations being single nucleotide substitutions distributed throughout the gene," wrote E. Berber and colleagues, Queen's University.
The authors continued, "Complicating the molecular characterization of this...
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Source: Blood Weekly (2006-10-19)
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