LRRK2 mutations in Parkinson disease.

Article Details

Citation

Farrer M, Stone J, Mata IF, Lincoln S, Kachergus J, Hulihan M, Strain KJ, Maraganore DM

LRRK2 mutations in Parkinson disease.

Neurology. 2005 Sep 13;65(5):738-40.

PubMed ID
16157908 [ View in PubMed
]
Abstract

To determine the frequency of LRRK2 mutations in idiopathic Parkinson disease (PD), the authors studied 786 PD probands, 32 affected siblings, 1,044 unaffected siblings, and 278 unrelated controls. The authors designed allelic discrimination assays for nine LRRK2 mutations and identified these in six probands with PD, one affected sibling, one unaffected sibling, and one unrelated control. Thus LRRK2 mutations only rarely cause idiopathic PD.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Leucine-rich repeat serine/threonine-protein kinase 2Q5S007Details