Parkinson disease LRRK2 gene mutation 12p11.23-q13.11 (Q95984): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 11:49, 16 August 2026
LRRK2 mutation is responsible for approximately 2 percent of the apparently sporadic PD in the western world and up to 30% in Northern African populations. It is inherited as a autosomal dominant trait.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_920819080 |
||
| English | Parkinson disease LRRK2 gene mutation 12p11.23-q13.11 |
LRRK2 mutation is responsible for approximately 2 percent of the apparently sporadic PD in the western world and up to 30% in Northern African populations. It is inherited as a autosomal dominant trait. |
Statements
CID11:ID_920819080
0 references
dki-india-ID_920819080
0 references
Concluído
0 references
15 August 2026
0 references
