Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene.

Hemochromatosis (HC) is a common inherited disorder of iron metabolism for which neither the gene nor biochemical defect have yet been identified. The aim of this study was to look for clinical evidence that the predominant ancestral haplotype in Australian patients is associated with a common mutat...

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Autori principali: Crawford, D H, Powell, L W, Leggett, B A, Francis, J S, Fletcher, L M, Webb, S I, Halliday, J W, Jazwinska, E C
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1995
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801553/
https://ncbi.nlm.nih.gov/pubmed/7668262
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