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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Detalles Bibliográficos
Autores principales: Sadhukhan, Dipanwita, Biswas, Arindam, Bhaduri, Arunima, Sarkar, Neelanjana, Biswas, Atanu, Das, Shyamal K., Banerjee, Tapas K., Ray, Kunal, Ray, Jharna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7602925/
https://www.ncbi.nlm.nih.gov/pubmed/32719233
http://dx.doi.org/10.4103/ijmr.IJMR_25_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7602925/
https://www.ncbi.nlm.nih.gov/pubmed/32719233
http://dx.doi.org/10.4103/ijmr.IJMR_25_18

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