@article{discovery1544814,
            year = {2017},
           month = {January},
          number = {1},
           title = {Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease},
           pages = {2--5},
          volume = {140},
            note = {This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.},
       publisher = {OXFORD UNIV PRESS},
         journal = {Brain},
            issn = {1460-2156},
        keywords = {Science \& Technology, Life Sciences \& Biomedicine, Clinical Neurology, Neurosciences, Neurosciences \& Neurology, Mitophagy},
             url = {http://doi.org/10.1093/brain/aww320},
          author = {Gandhi, S and Plun-Favreau, H},
        abstract = {This scientific commentary refers to
'Heterozygous PINK1 p.G411S increases
risk of Parkinson's disease
via a dominant-negative mechanism',
by Puschmann et al. (doi:10.1093/
brain/aww261).}
}