The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot.

Abstract

Am J Med Genet Part B 171: 925-930 25 April 2016, DOI: 10.1002/ajmg.b.32452 The above mentioned article was mistakenly published in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics in the Special Issue “Family, Twin and Adoption Studies of Childhood Onset Psychiatric and Neurodevelopmental Disorders,” Volume 171, Issue 7, October 2016, Pages 925–930. This article was intended to appear in the Special Issue “Genetic Factors in Neurodegenerative Diseases,” which is to be published in Am J Med Genet Part B 174:1, January 2017. The following link will direct you to the appropriate special issue: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.b.v174.1/issuetoc The publisher regrets this error.