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Medical Definition of Familial Parkinson disease type 3

Familial Parkinson disease type 3: A familial form of Parkinson disease inherited in an autosomal dominant manner due to a gene on chromosome 2p13. Also known as PARK3.

Source: MedTerms™ Medical Dictionary
https://www.medicinenet.com/script/main/art.asp?articlekey=25836
Last Editorial Review: 9/14/2016

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