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Genetic disorders can be inherited from our parents or mutations can occur in the human body to creating them.
Familial Hypercholesterolemia (FH) Arrays I & II are unique biochip assays that permit high discrimination between multiple targets in a number of genes.
The arrays enable detection of the most frequently occurring mutations known to cause disease (FH). A unique primer set is designed for each target which will hybridise to a complementary oligo-nucleotide probe spotted on a biochip discrete test region (DTR).