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CACNA1H mutant gene and how to detect childhood absence epilepsy-associated gene CACNA1H mutant gene

机译:CACNA1H突变基因以及如何检测儿童缺席癫痫相关基因CACNA1H突变基因

摘要

Relates to a method for detecting the CACNA1H mutant gene, one of childhood absence epilepsy-related gene, the method described restriction endonuclease or sequencing by direct invention, - a zero method relates CACNA1H mutant gene, wherein further at the same time on the application of this kit and detection kit of the mutant gene. It should be noted that the present invention relates to the application of the mutant gene and the detection method. In connection with the drug treatment of childhood absence epilepsy the CACNA1H gene provides a new target for drug treatment of this disease, the present invention, CACNA1H gene and Whipple's disease systemic epilepsy types of outside and childhood absence epilepsy at the same time I want to establish a basis for research and development of new drugs of strains of disease outside related to.
机译:涉及一种检测CACNA1H突变基因的方法,该基因是儿童缺席癫痫相关基因之一,该方法描述了限制性核酸内切酶或通过直接发明测序的方法;-一种零方法涉及CACNA1H突变基因,其中进一步在同时应用该试剂盒和突变基因检测试剂盒。应当注意,本发明涉及突变基因的应用和检测方法。与儿童期失神癫痫的药物治疗有关,CACNA1H基因为该疾病的药物治疗提供了新的靶点,我想同时建立本发明,CACNA1H基因和外部和儿童期失神癫痫的Whipple病全身性癫痫类型研发新的与疾病有关的新药的基础。

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