An update of the mutation profile of Factor 13 A and B genes

Arijit Biswas1, Vytautas Ivaskevicius, Rainer Seitz

  • 1Institute of Experimental Hematology and Transfusion Medicine, University Clinic Bonn, Germany. arijit.Biswas@ukb.uni-bonn.de

Blood Reviews
|June 7, 2011
PubMed

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Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...
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