Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome.
Year: 1999
Type: article
Source: PubMed
Authors: M Cicilano, G Zecchina, A Roetto, S Bosio, V Infelise, S Stefani, U Mazza, C Camaschella
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2187335510