Mutations in the Sphingolipid Pathway Gene SPTLC1 Are a Cause of Amyotrophic Lateral Sclerosis
Johnson O. Janel,Ruth Chia,Ravindran Kumaran,Nada Alahmady,Yevgeniya Abramzon,Faraz Faghri,Alan Renton,Simon D. Topp,Hannah A. Pliner,J. Raphael Gibbs,Jinhui Ding,Nathan Smith,Natalie Landeck,Michael A. Nalls,Mark R. Cookson,Olga Pletnikova,Juan Troncoso,Sonja W. Scholz,Marya S. Sabir,Sarah Ahmed,Clifton L. Dalgard,Claire Troakes,Ashley R. Jones,Aleksey Shatunov,Alfredo Iacoangeli,Ahmad Al Khleifat,Nicola Ticozzi,Vincenzo Silani,Cinzia Gellera,Ian P. Blair,Carol Dobson-Stone,John B. Kwok,Bryce K. England,The International ALS Genomics Consortium, The ITALSGEN Consortium,The FALS Sequencing Consortium,The American Genome Center,Pentti Tienari,David J. Stone,Karen E. Morrison,Pamela J. Shaw,Ammar Al-Chalabi,Robert H. Brown Jr.,Maura Brunetti,Andrea Calvo,Gabriele Mora,Marc Gotkine,Chris Shaw,John E. Landers,Adriano Chiò,Thomas O. Crawford,Bradley Smith,Bryan J. Traynor SSRN Electronic Journal（2019）
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