Parkinson disease UCHL-1 gene mutations 4p14 (Q95983): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
Revision as of 11:49, 16 August 2026
Mutations in ubiquitin carboxyterminal hydrolase L1 (UCHL-1) lead to dysfunction of the ubiquitin proteasome system. It has been hypothesized that UCHL-1 gene mutations on chromosome 4p14 may contribute to the etiology of Parkinson's disease due to reduced removal of synuclein by proteasomes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1067231592 |
||
| English | Parkinson disease UCHL-1 gene mutations 4p14 |
Mutations in ubiquitin carboxyterminal hydrolase L1 (UCHL-1) lead to dysfunction of the ubiquitin proteasome system. It has been hypothesized that UCHL-1 gene mutations on chromosome 4p14 may contribute to the etiology of Parkinson's disease due to reduced removal of synuclein by proteasomes. |
Statements
CID11:ID_1067231592
0 references
dki-india-ID_1067231592
0 references
Concluído
0 references
