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Discovery of a novel shared variant among RTEL1 Gene and RTEL1-TNFRSF6B lncRNA at chromosome 20q13.33 in familial progressive myoclonus epilepsy

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dc.contributor.author Chaudhari, Sima
dc.contributor.author Acharya, Lavanya Prakash
dc.contributor.author Jasti, Dushyanth Babu
dc.contributor.author Ware, Akshay Pramod
dc.contributor.author Gorthi, Sankar Prasad
dc.contributor.author Satyamoorthy K.
dc.date.accessioned 2025-01-26T05:15:08Z
dc.date.available 2025-01-26T05:15:08Z
dc.date.issued 2024-08
dc.identifier.citation International Journal of Genomics. 2024 Aug; 1-15. en_US
dc.identifier.issn 2314-4378
dc.identifier.uri http://dspace.sdmucmsh.edu.in:8080/xmlui/handle/123456789/2405
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Mitochondrial genome sequencing en_US
dc.subject Progressive myoclonic epilepsy en_US
dc.title Discovery of a novel shared variant among RTEL1 Gene and RTEL1-TNFRSF6B lncRNA at chromosome 20q13.33 in familial progressive myoclonus epilepsy en_US
dc.type Article en_US


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