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1986•Journal of Inherited Metabolic DiseaseRequires access

GM2 gangliosidosis with hexosaminidase A and B defect: Report of a family with motor neuron disease‐like phenotype

Antonio Federico, G. Ciacci, I D'Amore, Roberto Pallini, Silvia Palmeri, Alessandro Rossi, N. Rizzuto, G. C. Guazzi

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Key concepts: Studio, Humanities, Medicine, Art, Visual arts

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GM2 gangliosidosis with hexosaminidase A and B defect: Report of a family with motor neuron disease‐like phenotype — Research Paper | ScholarLens