Associated Papers
Similarities and Differences in the Late-Onset GM2 Gangliosidoses: Tay-Sachs and Sandhoff Diseases.
Lewis CJ et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
40970120 (PubMed )
Supplement: media-1.xlsx › HEXA
Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.
Sheth J et al.
Molecular Genetics and Metabolism Reports, 2014
Multiplexed fluorescence analysis for mutations causing Tay-Sachs disease.
Stockley TL et al.
Methods in Molecular Biology (clifton, N.j.), 2003
Biochemical consequences of mutations causing the GM2 gangliosidoses.
Mahuran DJ
Biochimica Et Biophysica Acta, 1999
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