Mutation analysis and association studies of the UCHL1 gene in German Parkinsonʼs disease patients-Reference-Cited by-同舟云学术

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Mutation analysis and association studies of the UCHL1 gene in German Parkinsonʼs disease patients

Published:2000-07 Issue:10 Volume:11 Page:2079-2082
ISSN:0959-4965
Container-title:NeuroReport
language:en
Short-container-title:NeuroReport

Author:

Wintermeyer Philip,Krüger Rejko,Kuhn Wilfried,Müller Thomas,Woitalla Dirk,Berg Daniela,Becker Georg,Leroy Elisabeth,Polymeropoulos Mihael,Berger Klaus,Przuntek Horst,Schöls Ludger,Epplen Jörg T.,Riess Olaf

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Neuroscience

Reference9 articles.

1. Pathology and Biology of the Lewy Body

2. Genetic dissection of familial Parkinson's disease

3. Substrate Specificity of Deubiquitinating Enzymes: Ubiquitin C-Terminal Hydrolases

4. GENEPOP (Version 1.2): Population Genetics Software for Exact Tests and Ecumenicism

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1. Ubiquitin Carboxyl-Terminal Hydrolase L1 and Its Role in Parkinson’s Disease;International Journal of Molecular Sciences;2024-01-21

2. Gene Signals and SNPs Associated with Parkinson’s Disease: A Nutrigenomics and Computational Prospective Insights;Neuroscience;2023-11

3. Genetic architecture of Parkinson’s disease;Биохимия;2023-03-15

4. Genetic Architecture of Parkinson’s Disease;Biochemistry (Moscow);2023-03

5. Role of Deubiquitinases in Parkinson’s Disease—Therapeutic Perspectives;Cells;2023-02-17

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