genes associated with hearing loss in the Japanese population

Growth of a brand new DHPLC assay for genotyping UGT1A (TA)n polymorphism related to Gilbert’s syndrome. BACKGROUND Gilbert’s syndrome is the most typical hereditary dysfunction of bilirubin metabolism. The causative mutation in Caucasians is sort of completely a (TA) dinucleotide insertion within the UGT1A1 promoter. Affected people are homozygous for the variant promoter and have 7 TA […]

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