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
Publicado en:Indian J Med Res
Main Authors: Sadhukhan, Dipanwita, Biswas, Arindam, Bhaduri, Arunima, Sarkar, Neelanjana, Biswas, Atanu, Das, Shyamal K., Banerjee, Tapas K., Ray, Kunal, Ray, Jharna
Formato: Artigo
Idioma:Inglês
Publicado: Wolters Kluwer - Medknow 2020
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Original Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7602925/
https://ncbi.nlm.nih.gov/pubmed/32719233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijmr.IJMR_25_18
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