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ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyDegenerative DiseaseZc4h2 MutationsMedical GeneticsDisease Gene IdentificationMedicineSynaptic SignalingArthrogryposis Multiplex Congenita