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Scientific Reports|May 17, 2022
CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainateToshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo, et al.
Plos One|March 4, 2014
Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defectsEmilie A Bard-Chapeau, Dorota Szumska, Bindya Jacob, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Nature Genetics|May 26, 2015
Transcriptional regulator PRDM12 is essential for human pain perceptionYa-Chun Chen, Michaela Auer-Grumbach, Shinya Matsukawa, et al.
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