Molecular analysis of HEXA gene in Argentinean patients affected with Tay–Sachs disease: Possible common origin of the prevalent c.459 + 5A>G mutation
Keywords: ACTR1a, alpha-centractin; AFAP, actin filament-associated protein; ALB, albumin; ME, Maximum Entropy; MLPA, Multiplex Ligation-dependent Probe Amplification; NN, Neural Network; PDB, Protein Data Bank; SD, Sandhoff diseaseGM2 gangliosidosis; Mutational an