Tissue typing for HFE mutations [2]

Hepatology

Volumn 35, Issue 4, 2002, Pages 977-978

  Raaka, Stuart ^a   Huehnergarth, Kier V ^a   Kowdley, Kris V ^a   Bronner, Mary P ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA EXTRACTION; GENE AMPLIFICATION; GENE MUTATION; GENETIC DISORDER; GENOTYPE; HEMOCHROMATOSIS; HUMAN; LETTER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TISSUE TYPING; VIRUS PURIFICATION;

HISTOCOMPATIBILITY ANTIGENS CLASS I; HISTOCOMPATIBILITY TESTING; HLA ANTIGENS; HUMANS; MEMBRANE PROTEINS; MUTATION;

EID: 0036203199     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1053/jhep.2002.32147     Document Type: Letter

References (10)

1. A novel MHC class I-like gene is mutated in patients with hereditary haemachromatosis
2. Recovering DNA and optimizing PCR conditions from microdissected formalin-fixed and paraffin-embedded material
3. Quantitative molecular analysis of laser-microdissected paraffin-embedded human tissues
4. Highthroughput DNA extraction from old paraffin-embedded biopsies
5. Direct multiplex amplification of DNA from a formalin fixed, paraffin wax embedded tissue section
6. Extraction of DNA from paraffin-embedded tissue for analysis by polymerase chain reaction: New tricks from an old friend
7. Modifications of human and viral deoxyribonucleic acid by formaldehyde fixation
8. PCR in situ: Aspects which reduce amplification and generate false positive results
9. Mutation analysis in hereditary hemochromatosis
10. Reply: Non-alcoholic steatohepatitis with iron: Part of insulin resistance-associated hepatic iron overload