Associated Papers
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability.
Moncini S et al.
Journal of Human Genetics, 2016
Effects of p35 Mutations Associated with Mental Retardation on the Cellular Function of p35-CDK5.
Takada S et al.
Plos One, 2015
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation.
Venturin M et al.
Neurogenetics, 2006
The reelin pathway components disabled-1 and p35 in gangliogliomas--a mutation and expression analysis.
Kam R et al.
Neuropathology and Applied Neurobiology, 2004
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