A Common 1317TC Polymorphism in MTHFR Can Lead to Erroneous 1298AC Genotyping by PCR-RE and TaqMan® Probe Assays
Author:
Affiliation:
1. Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
2. Department of Pathology, Creighton University Medical Center, Omaha, Nebraska.
Publisher
Mary Ann Liebert Inc
Subject
Genetics(clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/gte.2006.0513
Reference14 articles.
1. Low Frequency of Mutated Methylenetetrahydrofolate Reductase 677 C→T and 1298 A→C Genetics Single Nucleotide Polymorphisms (SNPs) in Sub-Saharan Populations
2. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing
3. Erroneous assignment of Gaucher disease genotype as a consequence of a complete gene deletion
4. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
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