Prevalence of the LRRK2 G2019S Mutation in a UK Community Based Idiopathic Parkinson's Disease Cohort

Journal of Neurology, Neurosurgery and Psychiatry - United Kingdom
doi 10.1136/jnnp.2005.085019
Full Text
Abstract

Available in full text

Date
Authors
Publisher

BMJ

Related search

Clinical Heterogeneity of the LRRK2 G2019S Mutation

Archives of Neurology
2006English

LRRK2 Screening in a Canadian Parkinson's Disease Cohort

Canadian Journal of Neurological Sciences
MedicineNeurology
2007English

LRRK2 Pathobiology in Parkinson's Disease

Journal of Neurochemistry
BiochemistryMolecular NeuroscienceCellular
2014English

LRRK2 G2019S Mutation Attenuates Microglial Motility by Inhibiting Focal Adhesion Kinase

Nature Communications
AstronomyGeneticsMolecular BiologyBiochemistryChemistryPhysics
2015English

Prevalence of Chronic Kidney Disease in the Community Using Data From OxRen: A UK Population-Based Cohort Study

British Journal of General Practice
MedicineFamily Practice
2020English

Presynaptic Dysfunction in Parkinson's Disease: A Focus on LRRK2

Biochemical Society Transactions
Biochemistry
2012English

Neurite Collapse and Altered ER Ca2+ Control in Human Parkinson Disease Patient iPSC-Derived Neurons With LRRK2 G2019S Mutation

Stem Cell Reports
BiochemistryGeneticsDevelopmental BiologyCell Biology
2019English

Rab29 Activation of the Parkinson's Disease‐associated LRRK2 Kinase

EMBO Journal
ImmunologyMolecular BiologyBiochemistryMicrobiology NeuroscienceMedicineGenetics
2019English

Identification of a Japanese Family With LRRK2 p.R1441G-related Parkinson's Disease

Neurobiology of Aging
AgingGerontologyDevelopmental BiologyGeriatricsNeuroscienceNeurology
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy