Screening of ARX, CDKL5 and STXBP1 gene mutations in Malaysian paediatric patients with early-onset epileptic encephalopathy by HRM technique
Gene mutation is one of the etiologies of early-onset infantile Epileptic Encephalopathy (EE), an age-dependant seizure in infants which leads to brain defects. Previous studies have shown that several genes namely, Aristaless-related homeobox (ARX), Cyclindependent kinase-like 5 (CDKL5) and Syntaxi...
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| Format: | Thesis |
| Language: | English |
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2015
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| Online Access: | http://psasir.upm.edu.my/id/eprint/57600/1/FPSK%28m%29%202015%2022RR.pdf |