Expanding Data Collection for the MDSGene Database: X‐linked Dystonia‐Parkinsonism as Use Case Example-Reference-Cited by-同舟云学术

Expanding Data Collection for the MDSGene Database: X‐linked Dystonia‐Parkinsonism as Use Case Example

Published:2020-09-19 Issue:11 Volume:35 Page:1933-1938
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Pauly Martje G.¹²^ORCID,Ruiz López Marta¹³,Westenberger Ana¹,Saranza Gerard⁴,Brüggemann Norbert¹⁵^ORCID,Weissbach Anne¹²,Rosales Raymond L.⁶,Diesta Cid C.⁷,Jamora Roland D.G.⁸,Reyes Charles J.¹,Madoev Harutyun¹,Petkovic Sonja¹,Ozelius Laurie J.⁹,Klein Christine¹,Domingo Aloysius¹⁹¹⁰

Affiliation:

1. Institute of Neurogenetics University of Lübeck Lübeck Germany

2. Institute of Systems Motor Science University of Lübeck Lübeck Germany

3. Cruces University Hospital Barakaldo Bizkaia Spain

4. Edmond J. Safra Program in Parkinsonʼs Disease and the Morton and Gloria Shulman Movement Disorders Centre Toronto Western Hospital Toronto Ontario Canada

5. Department of Neurology University of Lübeck Lübeck Germany

6. Department of Neurology and Psychiatry Pontifical and Royal University of Santo Tomas and Hospital Manila Philippines

7. Department of Neuroscience Makati Medical Center Makati City Philippines

8. Department of Neurosciences College of Medicine‐Philippine General Hospital, University of the Philippines Manila Manila Philippines

9. Collaborative Center for X‐linked Dystonia Parkinsonism, Department of Neurology Massachusetts General Hospital Boston Massachusetts USA

10. Center for Genomic Medicine Massachusetts General Hospital Boston Massachusetts USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28289

Reference22 articles.

1. MDSGene: Closing Data Gaps in Genotype-Phenotype Correlations of Monogenic Parkinson’s Disease

2. The Unique Phenomenology of Sex-Linked Dystonia Parkinsonism (XDP, DYT3, “Lubag”)

3. Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review

4. Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin , PINK1 , DJ1: MDSGene Systematic Review

5. New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3)

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3. X-linked dystonia parkinsonism: epidemiology, genetics, clinical features, diagnosis, and treatment;Acta Neurologica Belgica;2022-11-23

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