• Characterization of glycan substrates accumulating in GM1 Gangliosidosis 

      Lawrence, Roger; van Vleet, Jeremy L.; Mangini, Linley; Harris, Adam; Martin, Nathan T.; Clark, Wyatt T.; Chandriani, Sanjay; LeBowitz, Jonathan H.; Giugliani, Roberto; D'Azzo, Alessandra; Yogalingam, Gouri; Crawford, Brett E. (2019) [Artigo de periódico]
      Introduction: GM1 gangliosidosis is a rare autosomal recessive genetic disorder caused by the disruption of the GLB1 gene that encodes β-galactosidase, a lysosomal hydrolase that removes β-linked galactose from the ...