+ Site Statistics
References:
54,258,434
Abstracts:
29,560,870
PMIDs:
28,072,757
+ Search Articles
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ PDF Full Text
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Translate
+ Recently Requested

Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations



Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations



Blood Cells, Molecules and Diseases 25(3-4): 166-169




(PDF emailed within 0-6 h: $19.90)

Accession: 046211976

Download citation: RISBibTeXText

PMID: 10575542

DOI: 10.1006/bcmd.1999.0242


Related references

Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis. American Journal of Human Genetics 56(2): 428-433, 1995

Analysis of hemochromatosis gene mutations in the Sicilian population: implications for survival and longevity. Archives of Gerontology and Geriatrics. Supplement 8: 35-42, 2004

Analysis of hemochromatosis gene mutations in patients with hemochromatosis phenotype by capillary electrophoresis and a new ELISA based technique. Gastroenterology 116(4 PART 2): A420, April, 1999

Systematic haplotype sharing analysis as an asymptotically efficient tool to find gene positions in regions with high haplotype conservation and in complex diseases, illustrated with fine mapping of genes on chromosome 6 in multiple sclerosis and hemochromatosis. Cytogenetics & Cell Genetics 88(3-4): 185, 2000

A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region. Human Genetics. 102(5): 517-525,, 1998

Analysis of HFE mutations and non-HFE gene mutations (TFR2 and SLC40A1) in patients with phenotypic hemochromatosis from the Basque Country. International Journal of Laboratory Hematology 38(1): E5-E7, 2016

Refinement of the genetic mapping of the hemochromatosis gene by use of haplotype sharing analysis, and application of this method to Multiple Sclerosis. American Journal of Human Genetics 65(4): A435, 1999

Haplotype Analysis of Hemochromatosis Gene Polymorphisms in Chronic Hepatitis C Virus Infection: A Case Control Study. Iranian Red Crescent Medical Journal 18(6): E24675, 2016

Haplotype analysis in European Smith-Lemli-Opitz syndrome patients reveals different origins and ages of common DHCR7 mutations. European Journal of Human Genetics 9(Supplement 1): C051, 2001

Implications of beta2-microglobulin gene mutations and polymorphisms for the expression of hemochromatosis phenotype. Hepatology 34(4 Pt 2): 504A, October, 2001

Genetic testing for HFE gene mutations related to hereditary hemochromatosis. Tecnologica. Map Supplement. Blue Cross and Blue Shield Association. Medical Advisory Panel: 20-25, 2002

Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene. Mayo Clinic Proceedings 77(6): 522-530, 2002

Iron related hemochromatosis (HFE) gene mutations in Friedreich Ataxia patients. Parkinsonism and Related Disorders 34: 71-72, 2016

Prevalence of hemochromatosis related HFE gene mutations in patients with acute myeloid leukemia. Leukemia Research 23(6): 597-598, 1999

Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on hemodialysis. Nephrology Dialysis Transplantation 16(6): A137, June, 2001