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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: Gangliosidosis, Sandhoff disease, Hexosaminidase, Tay-Sachs disease, Phenotype, Amyotrophic lateral sclerosis, Biology, Ataxia

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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