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Lafora Progressive Myoclonus Epilepsy Mutation and Polymorphism Database (RRID:SCR_002919)Copy Citation Copied
URL: http://projects.tcag.ca/lafora/
Proper Citation: Lafora Progressive Myoclonus Epilepsy Mutation and Polymorphism Database (RRID:SCR_002919)
Description: The Lafora database is a repository of information related to progressive myoclonus epilepsy mutation and polymorphism data. Users may view all mutations in the database(Mutations of EPM2A and NHLRC1(EPM2B)), click on individual exons for mutations, or search the database by keyword. Nucleotide and amino acids positions were assigned based on the GenBank reference sequence NM_005670 for EPM2A and NM_198586 for EPM2B. The data can be viewed using the XRT Table Browser, and where possible, links to external sources such as NCBI, PubMed are provided. At this time, the database is under development. The BioXRT (Cross-Referenced Tables) Table Browser is a highly configurable tool for viewing complex, table based information. The tables can be displayed using pre-set options, or customized to view arbitrary subsets of rows, columns or other features.
Abbreviations: Lafora Database
Synonyms: Lafora Progressive Myoclonus Epilepsy Mutation Polymorphism Database, The Lafora Progressive Myoclonus Epilepsy Mutation and Polymorphism Database, The Lafora Progressive Myoclonus Epilepsy Mutation Polymorphism Database
Resource Type: database, data repository, storage service resource, data or information resource, service resource
Keywords: epilepsy, epm2a, genetics, laforin, malin, mutation, myoclonus, nhlrc1(epm2b), polymorphism
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