Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Epilepsy and SYNGAP1[original query] |
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De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism. Biological psychiatry 2011 May 69 (9): 898-901. Hamdan Fadi F, Daoud Hussein, Piton Amélie, Gauthier Julie, Dobrzeniecka Sylvia, Krebs Marie-Odile, Joober Ridha, Lacaille Jean-Claude, Nadeau Amélie, Milunsky Jeff M, Wang Zhenyuan, Carmant Lionel, Mottron Laurent, Beauchamp Miriam H, Rouleau Guy A, Michaud Jacques |
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy. Seizure 2018 6 59 132-140. Kothur Kavitha, Holman Katherine, Farnsworth Elizabeth, Ho Gladys, Lorentzos Michelle, Troedson Christopher, Gupta Sachin, Webster Richard, Procopis Peter G, Menezes Manoj P, Antony Jayne, Ardern-Holmes Simone, Dale Russell C, Christodoulou John, Gill Deepak, Bennetts Bru |
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 |
Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations. Frontiers in genetics 2022 12 13 957915. Wang Yanxin, Lv Yuqiang, Li Zilong, Gao Min, Yang Xiaomeng, Li Yue, Shi Jianguo, Gao Zaifen, Liu Yi, Gai Zhongt |
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- Page last updated:May 06, 2024
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