Question:

Which gene is associated with autosomal dominant Parkinsonism?

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LRRK2 mutation → most common cause of inherited (autosomal dominant) Parkinson’s disease.
Updated On: May 22, 2025
  • UCHL1
  • LRRK2
  • TIMP2
  • UCHL3
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The Correct Option is B

Solution and Explanation

Mutations in the LRRK2 gene (Leucine-rich repeat kinase 2) are known to cause autosomal dominant forms of Parkinson's disease. It is the most common genetic cause of familial Parkinsonism and also occurs in sporadic cases.
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