Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.

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dc.contributor.authorde Villiers J.N.
dc.contributor.authorScholtz C.L.
dc.contributor.authorHoogendijk C.F.
dc.contributor.authorCawood E.J.
dc.contributor.authorKotze M.J.
dc.date.accessioned2011-05-15T15:59:11Z
dc.date.available2011-05-15T15:59:11Z
dc.date.issued1998
dc.description.abstract[No abstract available]
dc.description.versionArticle
dc.identifier.citationHuman genetics
dc.identifier.citation102
dc.identifier.citation1
dc.identifier.issn3406717
dc.identifier.urihttp://hdl.handle.net/10019.1/11047
dc.subjectHFE protein, human
dc.subjectHLA antigen
dc.subjectHLA antigen class 1
dc.subjectmembrane protein
dc.subjectarticle
dc.subjectgenetics
dc.subjecthemochromatosis
dc.subjecthuman
dc.subjectmajor histocompatibility complex
dc.subjectmolecular genetics
dc.subjectmutation
dc.subjectHemochromatosis
dc.subjectHistocompatibility Antigens Class I
dc.subjectHLA Antigens
dc.subjectHumans
dc.subjectMajor Histocompatibility Complex
dc.subjectMembrane Proteins
dc.subjectMolecular Sequence Data
dc.subjectMutation
dc.titleHuman gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
dc.typeArticle
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