@misc{indiciae850be259ce65,
  title = {Mutations in the SPTLC1 gene are a cause of amyotrophic lateral sclerosis that may be amenable to serine supplementation},
  author = {Johnson, J. O. and Chia, R. and Kumaran, R. and Alahmady, N. and Miller, D. E. and Abramzon, Y. and Faghri, F. and Renton, A. E. and Topp, S. D. and Pliner, H. A. and Gibbs, J. R. and Ding, J. and Smith, N. and Landeck, N. and Nalls, M. A. and Cookson, M. R. and Pletnikova, O. and Troncoso, J. and Scholz, S. W. and Sabir, M. S. and Ahmed, S. and Dalgard, C. L. and Troakes, C. and Jones, A. R. and Shatunov, A. and Iacoangeli, A. and Al Khleifat, A. and Ticozzi, N. and Silani, V. and Gellera, C. and Blair, I. P. and Dobson-Stone, C. and Kwok, J. B. and England, B. K. and Bonkowski, E. S. and The International ALS Genomics Consortium, and The ITALSGEN Consortium, and The FALS Sequencing Consortium,},
  year = {2019},
  doi = {10.1101/770339},
  url = {https://www.biorxiv.org/content/10.1101/770339v1},
  note = {Source identifier: 10.1101/770339}
}