Huntington disease-like phenotype in a patient with ANO3 mutation

Koya Kutty S ¹ , Mulroy E ² , Magrinelli F ³ , Di Lazzaro G ⁴ , Latorre A ² , Bhatia KP ⁵

¹ Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, United Kingdom; Department of Internal Medicine, International Islamic University Malaysia, Pahang, Malaysia. Electronic address: mmedkacang@gmail.com
² Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, United Kingdom
³ Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, United Kingdom; Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy
⁴ Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, United Kingdom; Department of Systems Medicine, Tor Vergata University of Rome, Rome, Italy
⁵ Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, WC1N 3BG, United Kingdom. Electronic address: k.bhatia@ucl.ac.uk

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.