KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

European Journal of Human Genetics, Published online: 05 September 2019; doi:10.1038/s41431-019-0497-zKIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

Source: European Journal of Human Genetics - September 4, 2019 Category: Genetics & Stem Cells Authors: Maartje Pennings Meyke I. Schouten Judith van Gaalen Rowdy P. P. Meijer Susanne T. de Bot Marjolein Kriek Christiaan G. J. Saris Leonard H. van den Berg Michael A. van Es Dick M. H. Zuidgeest Mariet W. Elting Jiddeke M. van de Kamp Karin Y. van Spaendonck Source Type: research