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METHOD FOR DETECTING FILAGGRIN GENE MUTATION FOR DIAGNOSING ATOPIC DERMATITIS

机译:用于诊断原子性皮肤炎的丝蛋白基因突变的检测方法

摘要

The present invention relates to a probe complementarily binding to a filaggrin gene mutation nucleic acid sequence, and a method for detecting a filaggrin gene mutation using the same. Specifically, by preparing a PNA probe complementarily binding to a filaggrin gene and employing fluorescence melting curve analysis (FMCA) using a difference in binding strength between a normal type and a mutation type to provide the convenience of being able to determine a filaggrin gene mutation simply, promptly, and accurately, aetiological factors of atopic dermatitis patients can be diagnosed, and especially, the likelihood of atopic dermatitis during infancy immediately after birth can be promptly diagnosed, thereby decreasing the disease rate.
机译:本发明涉及与丝聚蛋白基因突变核酸序列互补结合的探针,以及使用该探针检测丝聚蛋白基因突变的方法。具体地,通过制备与丝聚蛋白基因互补结合的PNA探针,并利用荧光熔解曲线分析(FMCA),利用正常类型和突变类型之间的结合强度差异,提供能够简单地确定丝聚蛋白基因突变的便利。可以迅速而准确地诊断出特应性皮炎患者的病因,尤其是可以迅速诊断出出生后婴儿期特应性皮炎的可能性,从而降低了发病率。

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