Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
<p>Abstract</p> <p>Background</p> <p>Hereditary haemochromatosis (HH) is a recessively-inherited disorder of iron over-absorption prevalent in Caucasian populations. Affected individuals for Type 1 HH are usually either homozygous for a cysteine to tyrosine amino acid s...
| Hoofdauteurs: | , |
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| Formaat: | Artikel |
| Taal: | English |
| Gepubliceerd in: |
BMC
2006-11-01
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| Reeks: | BMC Medical Genetics |
| Online toegang: | http://www.biomedcentral.com/1471-2350/7/81 |