Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.

Hemochromatosis (HH) is an inborn error of iron metabolism, frequent among Caucasians, characterized by progressive iron loading that, if untreated, causes high morbidity and death. HLA-H, a putative HH gene, has recently been isolated. The large majority of patients so far studied are homozygous fo...

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Detalhes bibliográficos
Main Authors: Carella, M, D'Ambrosio, L, Totaro, A, Grifa, A, Valentino, M A, Piperno, A, Girelli, D, Roetto, A, Franco, B, Gasparini, P, Camaschella, C
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1712480/
https://ncbi.nlm.nih.gov/pubmed/9106528
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