SLC40A1-R178G mutation and ferroportin disease

J Hepatol. 2011 Sep;55(3):730-731. doi: 10.1016/j.jhep.2011.01.024. Epub 2011 Feb 12.

Authors

Matthaios Speletas¹, Elias Onoufriadis², Anna Kioumi³, Anastasios E Germenis²

Affiliations

¹ Department of Immunology and Histocompatibility, University of Thessaly, Medical School, 41110 Biopolis, Larissa, Greece. Electronic address: maspel@med.uth.gr.
² Department of Immunology and Histocompatibility, University of Thessaly, Medical School, Larissa, Greece.
³ Hematology Department, Papageorgiou General Hospital, Thessaloniki, Greece.

PMID: 21320560
DOI: 10.1016/j.jhep.2011.01.024

No abstract available

Publication types

Letter
Comment

MeSH terms

Cation Transport Proteins / genetics*
Female
Ferritins / blood*
Humans
Iron Overload / genetics*
Male
Mutation*
Transferrin / metabolism*

Substances

Cation Transport Proteins
Transferrin
Ferritins