Understanding the role of genetic variability in LRRK2 in Indian population

Author:

Kishore Asha1,Ashok Kumar Sreelatha Ashwin2,Sturm Marc3,von-Zweydorf Felix45,Pihlstrøm Lasse6,Raimondi Francesco7,Russell Rob7,Lichtner Peter8,Banerjee Moinak9,Krishnan Syam1,Rajan Roopa110,Puthenveedu Divya Kalikavil1,Chung Sun Ju11,Bauer Peter3,Riess Olaf3,Gloeckner Christian Johannes45ORCID,Kruger Rejko1213,Gasser Thomas12,Sharma Manu2, ,

Affiliation:

1. Sree Chitra Tirunal Institute for Medical Science and Technology; Kerala India

2. Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry; University of Tübingen; Tübingen Germany

3. Institute of Medical Genetics and Applied Genomics; University of Tübingen; Tübingen Germany

4. German Center for Neurodegenerative Diseases (DZNE); Tübingen Germany

5. Institute for Ophthalmic Research, Center for Ophthalmology; University of Tübingen; Tübingen Germany

6. Department of Neurology; Oslo University Hospital; Oslo Norway

7. Cell Networks; University of Heidelberg; Heidelberg Germany

8. Institute of Human Genetics; Helmholtz Zentrum München; Neuherberg Germany

9. Rajiv Gandhi Centre for Biotechnology; Kerala India

10. All India Institute for Medical Sciences; New Delhi India

11. Department of Neurology; Asan Medical Center, University of Ulsan College of Medicine; Seoul Korea

12. Center of Neurology, and Hertie Institute for Clinical Brain Research; University Hospital; Tübingen Germany

13. LCSB, Luxembourg Centre for Systems Biology; University of Luxembourg, and Centre Hospitalier de Luxembourg (CHL); Luxembourg

Funder

Michael J. Fox Foundation

German Research Council

EU Joint Program-Neurodegenerative diseases

Multiple System Atrophy Coalition, USA

Luxembourg National Research Fund

National Centre of Excellence in Research on Parkinson's disease

PEARL programme

EU Framework Programme for Research and Innovation H2020

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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