![Man and woman standing by poster showing DNA](http://cdn-acquia.dundee.ac.uk/sites/default/files/styles/card/public/2022-02/PINK1_TOM_image_0.jpg?itok=imMnh1-6&h=2e111cc1)
Press release
Mutations in PINK1 are the second most frequent cause of autosomal recessive early-onset Parkinson’s disease.
Press release
Mutations in PINK1 are the second most frequent cause of autosomal recessive early-onset Parkinson’s disease.