Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Syndrome and GABRG2[original query] |
---|
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy. Epilepsy research 2003 Mar 53 (3): 196-200. Madia Francesca, Gennaro Elena, Cecconi Massimiliano, Buti Daniela, Capovilla Giuseppe, Dalla Bernardina Bernardo, Elia Maurizio, Ferrari Annarita, Fontana Elena, Gaggero Roberto, Giannotta Melania, Giordano Lucio, Granata Tiziana, La Selva Lorita, Luisa Lispi Maria, Santucci Margherita, Vanadia Francesca, Veggiotti Pierangelo, Vigliano Piernanda, Viri Maurizio, Dagna Bricarelli Franca, Bianchi Amedeo, Zara Federi |
Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures. Neuroscience letters 2005 Aug 383 (3): 220-4. Ito Minako, Ohmori Iori, Nakahori Tomoyuki, Ouchida Mamoru, Ohtsuka Yo |
Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+? Epilepsia 2009 Apr 50 (4): 953-6. Sijben Angelique E J, Sithinamsuwan Pasiri, Radhakrishnan Ashalata, Badawy Radwa A B, Dibbens Leanne, Mazarib Aziz, Lev Dorit, Lerman-Sagie Tally, Straussberg Rachel, Berkovic Samuel F, Scheffer Ingrid |
Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies. Journal of human genetics 2010 Jun 55 (6): 375-8. Shi Xiuyu, Huang Ming-Chih, Ishii Atsushi, Yoshida Shuichi, Okada Motohiro, Morita Kohtaro, Nagafuji Hiroshi, Yasumoto Sawa, Kaneko Sunao, Kojima Toshio, Hirose Shinic |
GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures. Pharmacogenetics and genomics 2013 Nov 23 (11): 605-10. Balan Shabeesh, Sathyan Sanish, Radha Saradalekshmi K, Joseph Vijai, Radhakrishnan Kurupath, Banerjee Moin |
Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population. Neurology India 2013 60 (6): 6. Gitaí LL, de Almeida DH, Born JP, Gameleira FT, de Andrade TG, Machado LC, Gitaí DL |
Association of GABAA Receptor Gene with Epilepsy Syndromes. Journal of molecular neuroscience : MN 2018 May . Bhat Musadiq Ahmad, Guru Sameer Ahmad, Mir Rashid, Waza Ajaz Ahmad, Zuberi Mariyam, Sumi Mamta Pervin, Bodeliwala Shaam, Puri Vinod, Saxena Alpa |
Clinical and genetic study of developmental and epileptic encephalopathy in Argentinean pediatric patients. Medicina 2022 12 82 (6): 856-865. Juanes Matías, Loos Mariana, Reyes Gabriela, Veneruzzo Gabriel, García Francisco Martín, Aschettino Giovanna, Calligaris Silvana, Martín María Eugenia, Foncuberta María Eugenia, Alonso Cristina N, Caraballo Roberto |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: