Establishing functional assessment-based and long-range PCR-based analytic methods to molecularly characterize genetic defects in TSC patients
碩士 === 長庚大學 === 醫學生物技術暨檢驗學系 === 100 === The mutations in TSC1 or TSC2 genes are main causes of tuberous sclerosis complex. TSC1 and TSC2 mutations result in a consequence that their corresponding proteins, hamartin and tuberin, respectively, cannot form a functional protein complex. Due to dysfuncti...
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| Format: | Others |
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2012
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| Online Access: | http://ndltd.ncl.edu.tw/handle/09363049315346085646 |