Characterization of glycan substrates accumulating in GM1 Gangliosidosis

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 non-reducing end of glycans. Deficiency of this catabolic enzyme leads to the lysosom...

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Detalles Bibliográficos
Autores principales: Lawrence, Roger, Van Vleet, Jeremy L., Mangini, Linley, Harris, Adam, Martin, Nathan, Clark, Wyatt, Chandriani, Sanjay, LeBowitz, Jonathan H., Giugliani, Roberto, d'Azzo, Alessandra, Yogalingam, Gouri, Crawford, Brett E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838976/
https://www.ncbi.nlm.nih.gov/pubmed/31720227
http://dx.doi.org/10.1016/j.ymgmr.2019.100524

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838976/
https://www.ncbi.nlm.nih.gov/pubmed/31720227
http://dx.doi.org/10.1016/j.ymgmr.2019.100524

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