Work

Two Dutch families with hereditary hyperferritinaemia-cataract syndrome and heterozygosity for an HFE-related haemochromatosis gene mutation.

Year: 2003

Type: article

Study design: Case Report

Source: PubMed

Authors: S Simsek, P W B Nanayakkara, J M F Keek, L M Faber, K F Bruin, G Pals

Institutions: Amsterdam University Medical Centers, Amsterdam UMC Location University of Amsterdam, University of Amsterdam

Language: English

Topic: Iron Metabolism and Disorders

Subfield: Hematology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2189449076

FWCI: 0.341

Cites: 26

Cited by: 10

Related to: 10