A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease-Reference-Cited by-同舟云学术

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

Published:2005-01 Issue:9457 Volume:365 Page:412-415
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Di Fonzo Alessio,Rohé Christan F,Ferreira Joaquim,Chien Hsin F,Vacca Laura,Stocchi Fabrizio,Guedes Leonor,Fabrizio Edito,Manfredi Mario,Vanacore Nicola,Goldwurm Stefano,Breedveld Guido,Sampaio Cristina,Meco Giuseppe,Barbosa Egberto,Oostra Ben A,Bonifati Vincenzo

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. Unraveling the pathogenesis of Parkinson's disease—the contribution of monogenic forms;Bonifati;Cell Mol Life Sci,2004

2. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1;Funayama;Ann Neurol,2002

3. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004

4. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004

5. What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study;Hughes;Neurology,1992

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