Pub. Date : 2018 Dec
PMID : 30555092
7 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Identification of a novel GLB1 mutation in a consanguineous Pakistani family affected by rare infantile GM1 gangliosidosis. | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |
| 2 | Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (beta-Gal) encoded by galactose beta 1 (GLB1). | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |
| 3 | Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (beta-Gal) encoded by galactose beta 1 (GLB1). | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |
| 4 | Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (beta-Gal) encoded by galactose beta 1 (GLB1). | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |
| 5 | Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (beta-Gal) encoded by galactose beta 1 (GLB1). | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |
| 6 | Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (beta-Gal) encoded by galactose beta 1 (GLB1). | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |
| 7 | Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (beta-Gal) encoded by galactose beta 1 (GLB1). | G(M1) Ganglioside | galactosidase beta 1 | Homo sapiens |