Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
April 3, 2008European Journal of Gastroenterology & Hepatology

The biochemical and clinical penetrance of individuals diagnosed with genetic haemochromatosis by predictive genetic testing

View Full Paper
Ask AI
Bookmark
Share

Authors

SWStuart WatkinsInterventional CardiologyDTDouglas ThorburnNational Health ServiceNJNeeraj JoshiVanderbilt University Medical Center

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Watkins et al. (2008) studied this question.

synapsesocial.com/papers/6ab47bb7dac88c3fd5fd6e14https://doi.org/10.1097/meg.0b013e3282f3e708
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Should We Screen for Hemochromatosis?2002 · 16 citations
  2. 2Clinical expression of haemochromatosis in Irish C282Y homozygotes identified through family screening2004 · 51 citations
  3. 3Penetrance of the C28Y/C282Y genotype of theHFEgene2007 · 28 citations
  4. 4Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients2005 · 62 citations
  5. 5The prevalence of haemochromatosis gene mutations in the West of Scotland and their relation to ischaemic heart disease2003 · 37 citations