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Fatty liver in H63D homozygotes with hyperferritinemia

To study the clinical correlates of the H63D mu-tation we have analysed the phenotype of H63D homo-zygotes identified through mutation analysis in a referral laboratory. A total of 366 blood samples referred for HFE analysis were screened for C282Y and H63D mutations. Four H63D homozygotes were iden...

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Detalhes bibliográficos
Main Authors: Sebastiani, Giada, Wallace, Daniel F, Davies, Susan E, Kulhalli, Vasu, Walker, Ann P, Dooley, James S
Formato: Artigo
Idioma:Inglês
Publicado em: Baishideng Publishing Group Co., Limited 2006
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4124361/
https://ncbi.nlm.nih.gov/pubmed/16586555
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v12.i11.1788
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