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Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8

Neurodegenerative DiseasesMendelian DisorderAutosomal-recessive Intellectual DisabilityGenetic DisorderGeneticsDegenerative DiseaseNeuroscienceNeurologyCerebellar Atrophy SyndromeDisease Gene IdentificationNeuropathologyMedicineNeurogenetics