Frequency of the HFE C282Y and H63D mutations in distinct ethnic groups living in Spain.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

1. EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH).European journal of human genetics : EJHG · 2016
   Guideline
2. A Decreasing North-to-South Gradient ofGenes · 2026
   Article
3. The evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic.American journal of physical anthropology · 2016
   Article
4. Unique frequencies of HFE gene variants in Roma/Gypsies.Journal of applied genetics · 2012
   Article
5. Prevalence of 845G>A HFE mutation in Slavic populations: an east-west linear gradient in South Slavs.Croatian medical journal · 2011
   Article
6. Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?Gut · 2001
   Article

Corrections and comments

• Comment on
  Global prevalence of putative haemochromatosis mutations.1997

Authors and funding

3 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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