The SNCA (A53T, A30P, E46K) and LRRK2 (G2019S) mutations are rare cause of Parkinson's disease in South Indian patients

✍ Scribed by M. Vishwanathan Padmaja; Meenakshi Jayaraman; Avathvadi Venkatesan Srinivasan; C.R. Srikumari Srisailapathy; Arabandi Ramesh

• Book ID: 116821192
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 103 KB
• Volume: 18
• Category: Article
• ISSN: 1353-8020
• DOI: 10.1016/j.parkreldis.2012.02.012