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Volumn 270, Issue 4, 2013, Pages 1521-1529
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Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.
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Author keywords
[No Author keywords available]
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Indexed keywords
GAMMA INTERFERON;
INTERFERON GAMMA (1 39);
INTERFERON GAMMA (1-39);
ISOMERASE;
MACROPHAGE MIGRATION INHIBITION FACTOR;
MIF PROTEIN, HUMAN;
PEPTIDE FRAGMENT;
TUMOR NECROSIS FACTOR ALPHA;
ADOLESCENT;
ADULT;
AGED;
ALLELE;
ARTICLE;
COHORT ANALYSIS;
COMPARATIVE STUDY;
CULTURAL FACTOR;
DISEASE COURSE;
FEMALE;
GENETIC ASSOCIATION;
GENETIC PREDISPOSITION;
GENETICS;
HUMAN;
MALE;
MENIERE DISEASE;
MIDDLE AGED;
PERCEPTION DEAFNESS;
SINGLE NUCLEOTIDE POLYMORPHISM;
SPAIN;
UNITED STATES;
VERY ELDERLY;
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
ALLELES;
COHORT STUDIES;
CROSS-CULTURAL COMPARISON;
DISEASE PROGRESSION;
FEMALE;
GENETIC ASSOCIATION STUDIES;
GENETIC PREDISPOSITION TO DISEASE;
HEARING LOSS, SENSORINEURAL;
HUMANS;
INTERFERON-GAMMA;
INTRAMOLECULAR OXIDOREDUCTASES;
MACROPHAGE MIGRATION-INHIBITORY FACTORS;
MALE;
MENIERE DISEASE;
MIDDLE AGED;
PEPTIDE FRAGMENTS;
POLYMORPHISM, SINGLE NUCLEOTIDE;
SPAIN;
TUMOR NECROSIS FACTOR-ALPHA;
UNITED STATES;
YOUNG ADULT;
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EID: 84884756478
PISSN: None
EISSN: 14344726
Source Type: None
DOI: 10.1007/s00405-012-2268-0 Document Type: Article |
Times cited : (17)
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References (0)
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