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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jun 1, 2023. (Total: 217454Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Autosomal Dominant Partial Epilepsy With Auditory Features[original query]
Evaluation of depression risk in LGI1 mutation carriers.
Epilepsia 2010 Sep 51 (9): 1685-90.
Heiman Gary A, Kamberakis Kay, Gill Richard, Kalachikov Sergey, Pedley Timothy A, Hauser W Allen, Ottman Ru
A novel LGI1 missense mutation causes dysfunction in cortical neuronal migration and seizures.
Brain research 2019 7 1721 146332.
Liu Feng, Du Chao, Tian Xin, Ma Yuanlin, Zhao Bei, Yan Yin, Lin Zijun, Lin Peijia, Zhou Ruijiao, Wang Xuefe
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