Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism

Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism

Background & objectives: Parkinsonian disorder, including Parkinson's disease (PD), is an aetiologically complex neurodegenerative disorder. Mutations in leucine-rich repeat kinase 2 (LRRK2) gene have been implicated in an autosomal dominant form of PD with variable penetrance. The identifi...

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Bibliographic Details
Main Authors: Dipanwita Sadhukhan, Arindam Biswas, Arunima Bhaduri, Neelanjana Sarkar, Atanu Biswas, Shyamal K Das, Tapas K Banerjee, Kunal Ray, Jharna Ray
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Indian Journal of Medical Research
Subjects:
gly2019ser mutation - lrrk2 - parkinson plus - parkinson's disease - parkinsonism
Online Access:http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2020;volume=151;issue=6;spage=592;epage=597;aulast=Sadhukhan

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http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2020;volume=151;issue=6;spage=592;epage=597;aulast=Sadhukhan

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