HIF1A: A Putative Modifier of Hemochromatosis

HFE-related hereditary hemochromatosis (HH) is characterized by marked phenotypic heterogeneity. Homozygosity for p.C282Y is a low penetrance genotype suggesting that the HFE-HH is a multifactorial disease resulting from a complex interaction involving a major gene defect, genetic background and env...

Descripción completa

Detalles Bibliográficos
Autores principales: Pelucchi, Sara, Ravasi, Giulia, Arosio, Cristina, Mauri, Mario, Piazza, Rocco, Mariani, Raffaella, Piperno, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865586/
https://www.ncbi.nlm.nih.gov/pubmed/33513852
http://dx.doi.org/10.3390/ijms22031245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865586/
https://www.ncbi.nlm.nih.gov/pubmed/33513852
http://dx.doi.org/10.3390/ijms22031245

Ejemplares similares