Ferdowsi University of Mashhad
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Association of miR-132 and miR-185 Genes Methylation and their Expression Profile with Risk of Congenital Factor XIII Deficiency

Dor Mohammad Kordi-Tamandani; Zohreh Rezaei; Akbar Dorgalaleh-Mail

Volume 7, Issue 1 , July 2015, , Pages 19-25

https://doi.org/10.22067/jcmr.v7i1.38961

Abstract
  Congenital factor XIII deficiency is a very rare bleeding disorder, but because of the high rate of consanguineous marriages, it is common in Sistan and Baluchestan Province of Iran. The discovery of promoter hypermethylation of numerous miRNAs in human diseases has demonstrated an epigenetic mechanism ...  Read More