| Excerpt | Relevance | Reference |
|---|
| "Sandhoff disease (SD) is a lysosomal disease caused by a mutation of the HEXB gene associated with excessive accumulation of GM2 ganglioside (GM2) in lysosomes and neurological manifestations." | 7.77 | Thymic involution and corticosterone level in Sandhoff disease model mice: new aspects the pathogenesis of GM2 gangliosidosis. ( Itoh, K; Matsuoka, K; Taki, T; Tsuji, D, 2011) |
| "Sandhoff disease (SD) is a lysosomal disease caused by a mutation of the HEXB gene associated with excessive accumulation of GM2 ganglioside (GM2) in lysosomes and neurological manifestations." | 3.77 | Thymic involution and corticosterone level in Sandhoff disease model mice: new aspects the pathogenesis of GM2 gangliosidosis. ( Itoh, K; Matsuoka, K; Taki, T; Tsuji, D, 2011) |