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CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression
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ATXN1-CIC Complex Is the Primary Driver of Cerebellar Pathology in Spinocerebellar Ataxia Type 1 through a Gain-of-Function Mechanism. - Abstract - Europe PMC
CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression
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ATXN1L, CIC, and ETS Transcription Factors Modulate Sensitivity to MAPK Pathway Inhibition - ScienceDirect
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The New CIC Mutation Associates with Mental Retardation and Severity of Seizure in Turkish Child with a Rare Class I Glucose-6-Phosphate Dehydrogenase Deficiency | SpringerLink
Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1
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CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression
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