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Volumn 25, Issue 1, 2000, Pages 14-15
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The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
ARTICLE;
CHROMOSOME 7Q;
CLINICAL ARTICLE;
CONTROLLED STUDY;
GENE MAPPING;
GENE MUTATION;
GENETIC DISORDER;
GENOME;
HEMOCHROMATOSIS;
HUMAN;
IRON METABOLISM;
IRON OVERLOAD;
PEDIGREE ANALYSIS;
PRIORITY JOURNAL;
ANIMALS;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 7;
CODON, NONSENSE;
FEMALE;
HEMOCHROMATOSIS;
HUMANS;
MALE;
MICE;
MUTATION;
PEDIGREE;
RECEPTORS, TRANSFERRIN;
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EID: 0034022636
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/75534 Document Type: Article |
Times cited : (756)
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References (15)
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