Work

A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote☆

Year: 1999

Type: article

Source: Gastroenterology

DOI: 10.1016/s0016-5085(99)70505-6

Authors: D WALLACE, J DOOLEY, A WALKER

Institutions: The Royal Free Hospital, University College London

Language: English

Topic: Iron Metabolism and Disorders

Subfield: Hematology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

OpenAlex ID: W2013566167

FWCI: 12.96

Cites: 17

Cited by: 126

Related to: 10