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The C282Y Mutation Causing Hereditary Hemochromatosis Does Not Produce a Null Allele

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Year: 1999
Type: article
Source: Blood
DOI: 10.1182/blood.v94.1.9.413a43_9_11
Authors: Joanne E. Levy, Lynne K. Montross, Dena E. Cohen, Mark D. Fleming, Nancy C. Andrews
Institutions: Brigham and Women's Hospital, Howard Hughes Medical Institute, Harvard University
Language: English

Topic: Iron Metabolism and Disorders
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: National Heart, Lung, and Blood Institute
Awards: TRANSFERRIN RECEPTOR AND ERYTHROPOIESIS, MURINE IRON METABOLISM MUTATION MICROCYTOSIS (MK)
OpenAlex ID: W284603049
FWCI: 12.1
Cites: 10
Cited by: 260
Related to: 10
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