LRRK2 mutations and Parkinsonism

Publisher Website

1 April 2005

journal article
Published by Elsevier in The Lancet

Vol. 365 (9466), 1229-1230
https://doi.org/10.1016/s0140-6736(05)74809-1

Abstract

No abstract available

This publication has 2 references indexed in Scilit:

A frequent gene mutation associated with autosomal dominant Parkinson's disease
The Lancet, 2005
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Neuron, 2004

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