Parkinson disease-associated mutation R1441H in LRRK2 prolongs the "active state" of its GTPase domain-Reference-Cited by-同舟云学术

Parkinson disease-associated mutation R1441H in LRRK2 prolongs the "active state" of its GTPase domain

Published:2014-03-03 Issue:11 Volume:111 Page:4055-4060
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Liao J.,Wu C.-X.,Burlak C.,Zhang S.,Sahm H.,Wang M.,Zhang Z.-Y.,Vogel K. W.,Federici M.,Riddle S. M.,Nichols R. J.,Liu D.,Cookson M. R.,Stone T. A.,Hoang Q. Q.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference26 articles.

1. The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease

2. LRRK2 in Parkinson's disease: protein domains and functional insights

3. Mutations in LRRK2 as a Cause of Parkinson’s Disease

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

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

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