Literature DB >> 10545942

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.

A T Merryweather-Clarke, J J Pointon, J D Shearman, K J Robson, A M Jouanolle, A Mosser, V David, J Y Le Gall, D J Halsall, T S Elsey, A Kelly, T M Cox, M Clare, A Bomford, J L Vandwalle, J Rochette, N Borot, H Coppin, M P Roth, E Ryan, J Crowe, A Totaro, P Gasparini, A Roetto, A P Walker.   

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Year:  1999        PMID: 10545942     DOI: 10.1038/15452

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


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  4 in total

1.  Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

Authors:  E Cadet; D Capron; M Gallet; M-L Omanga-Léké; H Boutignon; C Julier; K J H Robson; J Rochette
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

2.  The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.

Authors:  K J Livesey; V L C Wimhurst; K Carter; M Worwood; E Cadet; J Rochette; A G Roberts; J J Pointon; A T Merryweather-Clarke; M L Bassett; A-M Jouanolle; A Mosser; V David; J Poulton; K J H Robson
Journal:  J Med Genet       Date:  2004-01       Impact factor: 6.318

3.  Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.

Authors:  K J H Robson; D J Lehmann; V L C Wimhurst; K J Livesey; M Combrinck; A T Merryweather-Clarke; D R Warden; A D Smith
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

4.  Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis.

Authors:  Caitriona King; David E Barton
Journal:  BMC Med Genet       Date:  2006-11-29       Impact factor: 2.103

  4 in total

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