Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease-Reference-Cited by-同舟云学术

Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease

Published:2006 Issue:12 Volume:21 Page:2257-2260
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Pankratz Nathan,Pauciulo Michael W.,Elsaesser Veronika E.,Marek Diane K.,Halter Cheryl A.,Rudolph Alice,Shults Clifford W.,Foroud Tatiana,Nichols William C.,

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference15 articles.

1. Genetics of Parkinsonʼs disease

2. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

3. Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*

4. Lrrk2 pathogenic substitutions in Parkinson's disease

5. Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

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