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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Syndrome and HCN1[original query]
Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Jan 150B (1): 95-103.
Laurin Nancy, Wigg Karen G, Feng Yu, Sandor Paul, Barr Cathy
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome.
Seizure 2019 2 66 26-30.
Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh
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