Pub. Date : 2022 Jul
PMID : 35533513
3 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Generation of gene-corrected isogenic control cell lines from a DYT1 dystonia patient iPSC line carrying a heterozygous GAG mutation in TOR1A gene. | Glycosaminoglycans | torsin family 1 member A | Homo sapiens |
| 2 | Childhood-onset torsin dystonia (DYT1) is a rare hereditary movement disorder and usually caused by a heterozygous GAG deletion (c.907-909) in the TOR1A gene (DeltaE, p.Glu303del). | Glycosaminoglycans | torsin family 1 member A | Homo sapiens |
| 3 | Childhood-onset torsin dystonia (DYT1) is a rare hereditary movement disorder and usually caused by a heterozygous GAG deletion (c.907-909) in the TOR1A gene (DeltaE, p.Glu303del). | Glycosaminoglycans | torsin family 1 member A | Homo sapiens |