Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Seizures and SLC2A1[original query] |
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| Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency. Epilepsia 2012 Dec 53 (12): e204-7. Arsov Todor, Mullen Saul A, Damiano John A, Lawrence Kate M, Huh Linda L, Nolan Melinda, Young Helen, Thouin Anaïs, Dahl Hans-Henrik M, Berkovic Samuel F, Crompton Douglas E, Sadleir Lynette G, Scheffer Ingrid |
| Genetic generalized epilepsies. Epilepsia 2018 5 59 (6): 1148-1153. Mullen Saul A, Berkovic Samuel F, |
| Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia. Epileptic disorders : international epilepsy journal with videotape 2018 Oct 20 (5): 396-400. Alt?okka-Uzun Güne?, Özdemir Özkan, U?ur-??eri Sibel, Bebek Nerses, Gürses Candan, Özbek U?ur, Baykan Bet |
| Dissecting the phenotypic and genetic spectrum of early childhood-onset generalized epilepsies. Seizure 2019 8 71 222-228. Kim Soo Yeon, Jang Se Song, Kim Jong-Il, Kim Hunmin, Hwang Hee, Choi Ji Eun, Chae Jong-Hee, Kim Ki Joong, Lim Byung Ch |
| SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. Human genetics 2021 11 141 (1): 81-99. Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous |
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