Catalog

Parkinson disease LRRK2 gene mutation 12p11.23-q13.11

No MMS code

Link to WHO Definition

Parkinson disease LRRK2 gene mutation 12p11.23-q13.11 – http://id.who.int/icd/entity/920819080

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.