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Medical Definition of Familial Parkinson disease type 5

Familial Parkinson disease type 5: A familial form of Parkinson disease inherited in an autosomal dominant manner due to mutation in the UCHL1 gene on chromosome 4p14. Also known as PARK5.

Source: MedTerms™ Medical Dictionary
http://www.medicinenet.com/script/main/art.asp?articlekey=25838
Last Editorial Review: 9/14/2016

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