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...
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| Format: | Book |
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BMC,
2006-11-01T00:00:00Z.
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A1234.567 |
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