Association Analysis of Candidate Variants in Admixed Brazilian Patients With Genetic Generalized Epilepsies.
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| Title: | Association Analysis of Candidate Variants in Admixed Brazilian Patients With Genetic Generalized Epilepsies. |
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| Authors: | Kaibara FS; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., de Araujo TK; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., Araujo PAORA; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., Alvim MKM; Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., Yasuda CL; Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., Cendes F; Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., Lopes-Cendes I; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil., Secolin R; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil. |
| Source: | Frontiers in genetics [Front Genet] 2021 Jul 08; Vol. 12, pp. 672304. Date of Electronic Publication: 2021 Jul 08 (Print Publication: 2021). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2021.672304 |
