Publication | Open Access

Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler–Scheie syndrome

Neurodegenerative DiseasesMolecular NeuroscienceNeurogenomicsNeurological Disorderα-L-iduronidase GeneGeneticsGenetic DisorderMutation L238qNeurologyNeuroscienceHurler–scheie SyndromeDisease Gene IdentificationMedicineSocial SciencesNeurogenetics