Publication | Open Access

A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I

Synaptic SignalingMolecular EtiologyGenetic DisorderGeneticsDegenerative DiseaseNeurologyMolecular NeurobiologyDisease Gene IdentificationKash DomainNeuropathologyMedicineNesprin1 Giant Devoid