The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease-Reference-Cited by-同舟云学术

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The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Published:2013-03-27 Issue:17 Volume:80 Page:1606-1610
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Gan-Or Z.,Ozelius L. J.,Bar-Shira A.,Saunders-Pullman R.,Mirelman A.,Kornreich R.,Gana-Weisz M.,Raymond D.,Rozenkrantz L.,Deik A.,Gurevich T.,Gross S. J.,Schreiber-Agus N.,Giladi N.,Bressman S. B.,Orr-Urtreger A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 150 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lysosomal dysfunction in α-synuclein pathology: molecular mechanisms and therapeutic strategies;Cellular and Molecular Life Sciences;2024-09-03

2. Prediction of motor and non-motor Parkinson’s disease symptoms using serum lipidomics and machine learning: a 2-year study;npj Parkinson's Disease;2024-06-25

3. Genome-wide association study of glucocerebrosidase activity modifiers.;2024-06-07

4. Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry;Journal of Movement Disorders;2024-04-30

5. Smpd1regulates chitin-clearance for tracheal gas-filling in theDrosophilaembryo in a ceramide-specific manner;2024-04-20

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