Presynaptic Dysfunction in Neurons Derived from Tay–Sachs iPSCs
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Inborn errors of metabolism: Lessons from iPSC models
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JCI Insight - Early defects in mucopolysaccharidosis type IIIC disrupt excitatory synaptic transmission
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3052 PDFs Review articles in TAY-SACHS DISEASE
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PDF) Presynaptic Dysfunction in Neurons Derived from Tay-Sachs-iPSCs
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Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
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Frontiers Aberrant Autophagy Impacts Growth and Multicellular Development in a Dictyostelium Knockout Model of CLN5 Disease
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A novel iPSC model reveals selective vulnerability of neurons in Multiple Sulfatase Deficiency
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Cells, Free Full-Text
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Biochemical Phenotype of GM1-iPSC-Derived Neural Stem Cells (A) b-GAL
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Analysis of M6PHexA uptake by TS and SD fibroblasts. (A) TS and SD
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A case of infantile Tay-Sachs disease with late onset spasms - ScienceDirect
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