Please use this identifier to cite or link to this item: https://libjncir.jncasr.ac.in/xmlui/handle/10572/813
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dc.contributor.advisorAnand, Anuranjan-
dc.contributor.authorRatnapriya, R.-
dc.date.accessioned2012-09-07T11:31:48Z-
dc.date.available2012-09-07T11:31:48Z-
dc.date.issued2009-
dc.identifier.citationRatnapriya, R. 2009, Identification of genetic loci for human epilepsies, Ph.D thesis, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluruen_US
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/813-
dc.descriptionOpen access-
dc.description.abstractEpilepsy is relatively common neurological disorder affecting 0.5-1% of population during their lifetime (Hauser et al., 1993; Kaneko et al., 2002). Epilepsy is characterized by usually unprovoked and recurrent seizures, which are consequence of intensive burst activity from groups of neurons. Epileptic seizures are usually intermittent, self-limiting and occur with or without loss of consciousness. Seizures are generalized when synchronized firing of neurons involves the whole brain, or focal wherein seizure activity is limited to a specific brain region. While final outcome of seizure results from many complex and interacting biological phenomenon, abnormal cellular excitability and neuronal network defects are considered the two major physiological elements underlying seizure activity of the brain.-
dc.language.isoEnglishen_US
dc.publisherJawaharlal Nehru Centre for Advanced Scientific Researchen_US
dc.rights© 2009 JNCASRen_US
dc.subjectHuman Epilepsiesen_US
dc.subjectMolecular Biologyen_US
dc.titleIdentification of genetic loci for human epilepsiesen_US
dc.typeThesisen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePh.D.en_US
dc.publisher.departmentMolecular Biology and Genetics Unit (MBGU)en_US
Appears in Collections:Student Theses (MBGU)

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