Molecular basis of movement disorders-Reference-Cited by-同舟云学术

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Molecular basis of movement disorders

Published:2020 Issue: Volume: Page:461-485
ISSN:
Container-title:Clinical Molecular Medicine
language:
Short-container-title:

Author:

MacIver Claire,Morgan Dafydd,Peall Kathryn J.

Publisher

Elsevier

Reference50 articles.

1. Genetics of Parkinson disease: paradigm shifts and future prospects;Farrer;Nat Rev Genet,2006

2. Autophagy in dementias;Kragh;Brain Pathol,2012

3. The synaptic function of LRRK2;Lee;Biochem Soc Trans,2012

4. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease;Zimprich;Am J Hum Genet,2011

5. Association between early-onset Parkinson’s disease and mutations in the parkin gene;Lücking;New Engl J Med,2000

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1. To the question of differentiation of ataxias (analytical review);Bulletin of the Medical Institute "REAVIZ" (REHABILITATION, DOCTOR AND HEALTH);2022-04-25

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