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HUMAN TOLL-LIKE RECEPTOR 3 GENE POLYMORPHISM AS MARKER FOR INHERITED FACTOR OF ALLERGIC DISEASE AND UTILIZATION OF THE SAME
HUMAN TOLL-LIKE RECEPTOR 3 GENE POLYMORPHISM AS MARKER FOR INHERITED FACTOR OF ALLERGIC DISEASE AND UTILIZATION OF THE SAME
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机译:像人类Toll样受体3基因多态性作为过敏性疾病和利用的遗传因素的标记
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摘要
An inherited factor for an allergic disease is examined by detecting the gene polymorphism at least one of single nucleotide polymorphism sites located at the -8921, -7, 1638, 1656, 3519, 4792, 4960, 5252, 6301 and 6444 positions in human Toll-like receptor 3 (TLR3) gene.
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