Article
Linked linear amplification for simultaneous analysis of the two most common hemochromatosis mutations.
Clinical chemistry - 1 Jul 2003
Killeen Anthony A, Breneman John W, Carillo Arlene R, Ugozzoli Luis A, Lowery Jimmie D, Liu Jason, Hixson Craig S
Abstract excerpt
BACKGROUND: Two mutations in HFE, G845A (amino acid substitution C282Y) and C187G (H63D), are associated with hereditary hemochromatosis. We developed and validated a novel method, linked linear amplification (LLA), for detection of these two mutations. METHODS: Two segments of HFE were amplified by a multiplex LLA reaction that generated biotinylated LLA products. Aliquots of the multiplex LLA reaction were...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
