HFE gene mutation and transferrin saturation in very low birthweight infants

AIM—To determine if there is an association between high transferrin saturation and the C282Y HFE gene mutation in very low birthweight (VLBW) infants.
METHODS—One hundred and forty three VLBW infants receiving recombinant erythropoietin and 3 to 9 mg/kg/day of enteral iron were studied. Genomic DNA...

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Autores principales: Maier, R., Witt, H., Buhrer, C., Monch, E., Kottgen, E.
Formato: Artigo
Lenguaje:Inglês
Publicado: BMJ Group 1999
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1720994/
https://ncbi.nlm.nih.gov/pubmed/10448186
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