APPLICATION OF GENETIC MODIFICATION IN A GENE FOR SUBUNIT OF {BETA}3 HUMAN G-PROTEIN FOR DIAGNOSIS OF DISEASES

摘要

The present invention relates to a method for determining risk of development of a disorder connected with replacement of cytosine with thymine in position 825 SEQ. ID. No.:1, whereby the invented method is characterized by identification of a genetic modification of a gene for subunit of the {beta}3 human G-protein.