Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families-Reference-Cited by-同舟云学术

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

Published:2007-01 Issue:1 Volume:22 Page:55-61
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Ishihara Lianna,Gibson Rachel A.,Warren Liling,Amouri Rim,Lyons Kelly,Wielinski Catherine,Hunter Christine,Swartz Jina E.,Elango Ramu,Akkari P. Anthony,Leppert David,Surh Linda,Reeves Kevin H.,Thomas Siwan,Ragone Leigh,Hattori Nobutaka,Pahwa Rajesh,Jankovic Joseph,Nance Martha,Freeman Alan,Gouider-Khouja Neziha,Kefi Mounir,Zouari Mourad,Ben Sassi Samia,Ben Yahmed Samia,El Euch-Fayeche Ghada,Middleton Lefkos,Burn David J.,Watts Ray L.,Hentati Faycal

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference35 articles.

1. Genetics of Parkinsonʼs disease

2. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1

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

4. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease

5. A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

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