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Parkinson Disease 6, Autosomal Recessive Early-Onset

Known as: Parkinson Disease 6, Early-Onset, PARKINSON DISEASE, AUTOSOMAL RECESSIVE EARLY-ONSET, DIGENIC, PINK1/DJ1, PARK6 
National Institutes of Health

Papers overview

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2017
2017
PRKN and PINK1 genes mutations represent the most common cause of autosomal recessive early onset Parkinson’s disease (EOPD). We… 
2015
2015
Mutations in parkin (PARK2), an ubiquitin ligase, cause early onset Parkinson's disease. Parkin was shown to bind, ubiquitinate… 
2012
2012
Neurodegenerative disorders, such as Parkinson’s diseases (PD), are characterized by loss of specific neuronal populations and… 
2008
2008
We have reported a case of autosomal recessive juvenile parkinsonism PARK6 with a 30-year history. She developed tremor of right… 
2006
2006
Background: Abnormalities of the parkin gene is the most frequently found genetic abnormality in patients with sporadic young age… 
Review
2001
Review
2001
A genetic contribution to the etiology of Parkinson's disease was first suspected by Charcot and later confirmed by case control…