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家族性中枢神经系统海绵状血管瘤的分子医学研究现状 被引量:1

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摘要 本文从当今分子医学的角度,介绍了中枢神经系统海绵状血管瘤(CCM)的研究现状。文章首先对CCM的致病基因所在染色体定位的研究加以综述,以使读者了解到目前对该病的分子遗传学研究过程。进而,又综述了人们根据分子遗传学研究结果所开展的CCM分子病理学实验室研究工作,并总结了对新发现基因Krit-1突变的认识和其热点外显子的特征,从而为研究CCM病因学、症状前基因诊断学、新发现抑癌基因的功能和基因治疗提供了一些思路。
出处 《国外医学(神经病学.神经外科学分册)》 2002年第4期369-372,共4页 Foreign Medical Sciences(Section On Neurology & Neurosurgery)
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同被引文献1

  • 1Hildegard Kehrer-Sawatzki,Monika Wilda,Veit M. Braun,Hans-Peter Richter,Horst Hameister. Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1)[J] 2002,Acta Neuropathologica(3):231~240

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