Large-Scale Screening forHFEMutations: Methodology and Cost
Author:
Affiliation:
1. Scripps Research Institute, Department of Molecular and Experimental Medicine, La Jolla, CA 92037.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/10906570050114830
Reference37 articles.
1. Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.
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4. G6PD deficiency
5. Erroneous assignment of Gaucher disease genotype as a consequence of a complete gene deletion
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