Browsing centerforsynapticbraindysfunctions시냅스뇌질환연구단 byKeyword : intellectualdisability
Showing results 1 to 3 of 3
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Publication Date2015-01
De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy
Jae-Ran Lee; Myriam Srour; Doyoun Kim, et al
HUMAN MUTATION, v.36, no.1, pp.69 - 78
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Publication Date2015-07
Mice lacking the synaptic adhesion molecule Neph2/Kirrel3 display moderate hyperactivity and defective novel object preference
Su-Yeon Choi; Kihoon Han; Tyler Cutforth, et al
FRONTIERS IN CELLULAR NEUROSCIENCE, v.9, no.JULY, pp.283
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Publication Date2019-06
Scn2a Haploinsufficiency in Mice Suppresses Hippocampal Neuronal Excitability, Excitatory Synaptic Drive, and Long-Term Potentiation, and Spatial Learning and Memory.
Wangyong Shin; Hanseul Kweon; Ryeonghwa Kang, et al
FRONTIERS IN MOLECULAR NEUROSCIENCE, v.12, pp.145 - 145
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