Literature DB >> 9577377

Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis.

D Baty1, A Terron Kwiatkowski, D Mechan, A Harris, M J Pippard, D Goudie.   

Abstract

Genetic testing for hereditary haemochromatosis is likely to be a significant workload for diagnostic laboratories. The C282Y and H63D mutations in the HFE gene associated with hereditary haemochromatosis have previously been detected using a number of methods including alterations in the restriction digest pattern of polymerase chain reaction (PCR) amplified products. An amplification refractory mutation system (ARMS) has been developed that will simultaneously detect both hereditary haemochromatosis mutations. Comparison of the results obtained from the analysis of 46 samples referred for hereditary haemochromatosis testing showed no discrepancies between ARMS and restriction enzyme digestion. Furthermore, consistent results were obtained by ARMS from both blood and buccal mouthwash samples. The ARMS test is quicker and less expensive in terms of consumables and scientist time than restriction enzyme analysis, and is therefore suited to the routine diagnostic analysis of hereditary haemochromatosis.

Entities:  

Mesh:

Year:  1998        PMID: 9577377      PMCID: PMC500436          DOI: 10.1136/jcp.51.1.73

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  12 in total

1.  Global prevalence of putative haemochromatosis mutations.

Authors:  A T Merryweather-Clarke; J J Pointon; J D Shearman; K J Robson
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  Cystic fibrosis mutation analysis: report from 22 U.K. regional genetics laboratories.

Authors:  M J Schwarz; G M Malone; A Haworth; J P Cheadle; A L Meredith; A Gardner; I H Sawyer; M Connarty; N Dennis; A Seller
Journal:  Hum Mutat       Date:  1995       Impact factor: 4.878

3.  Haemochromatosis and HLA-H.

Authors:  E C Jazwinska; L M Cullen; F Busfield; W R Pyper; S I Webb; L W Powell; C P Morris; T P Walsh
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

4.  Haemochromatosis and HLA-H.

Authors:  A M Jouanolle; G Gandon; P Jézéquel; M Blayau; M L Campion; J Yaouanq; J Mosser; P Fergelot; B Chauvel; P Bouric; G Carn; N Andrieux; I Gicquel; J Y Le Gall; V David
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

5.  Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

Authors:  C R Newton; A Graham; L E Heptinstall; S J Powell; C Summers; N Kalsheker; J C Smith; A F Markham
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

6.  The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance.

Authors:  N E Kirschbaum; P A Foster
Journal:  Thromb Haemost       Date:  1995-09       Impact factor: 5.249

7.  Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda.

Authors:  A G Roberts; S D Whatley; R R Morgan; M Worwood; G H Elder
Journal:  Lancet       Date:  1997-02-01       Impact factor: 79.321

8.  Mutation analysis in hereditary hemochromatosis.

Authors:  E Beutler; T Gelbart; C West; P Lee; M Adams; R Blackstone; P Pockros; M Kosty; C P Venditti; P D Phatak; N K Seese; K A Chorney; A E Ten Elshof; G S Gerhard; M Chorney
Journal:  Blood Cells Mol Dis       Date:  1996       Impact factor: 3.039

9.  Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene.

Authors:  R M Ferrie; M J Schwarz; N H Robertson; S Vaudin; M Super; G Malone; S Little
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

10.  Long-term survival in patients with hereditary hemochromatosis.

Authors:  C Niederau; R Fischer; A Pürschel; W Stremmel; D Häussinger; G Strohmeyer
Journal:  Gastroenterology       Date:  1996-04       Impact factor: 22.682

View more
  4 in total

1.  Efficient recovery of DNA from peripheral blood for diagnostic analysis with a vacuum manifold.

Authors:  S M Kukuczka; L E Grosso
Journal:  Mol Diagn       Date:  2000-06

2.  Effect of hereditary haemochromatosis genotypes and iron overload on other trace elements.

Authors:  Jeffrey M Beckett; Madeleine J Ball
Journal:  Eur J Nutr       Date:  2012-02-09       Impact factor: 5.614

3.  Detection of hemochromatosis through the analysis of single- nucleotide extension products by capillary electrophoresis.

Authors:  Q Liang; P A Davis; J T Simpson; B H Thompson; J M Devaney; J Girard
Journal:  J Biomol Tech       Date:  2000-06

4.  Total mortality by elevated transferrin saturation in patients with diabetes.

Authors:  Christina Ellervik; Henrik Ullits Andersen; Anne Tybjærg-Hansen; Merete Frandsen; Henrik Birgens; Børge G Nordestgaard; Thomas Mandrup-Poulsen
Journal:  Diabetes Care       Date:  2013-06-25       Impact factor: 19.112

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.