Mutations in the SPTLC1 gene are a cause of amyotrophic lateral sclerosis that may be amenable to serine supplementation

Added 26 days ago (20.09.2019)
Authors: Johnson, J. O., Chia, R., Kumaran, R., Alahmady, N., Miller, D. E., Abramzon, Y., Faghri, F., Renton, A. E., Topp, S. D., Pliner, H. A., Gibbs, J. R., Ding, J., Smith, N., Landeck, N., Nalls, M. A., Cookson, M. R., Pletnikova, O., Troncoso, J., Scholz, S. W., Sabir, M. S., Ahmed, S., Dalgard, C. L., Troakes, C., Jones, A. R., Shatunov, A., Iacoangeli, A., Al Khleifat, A., Ticozzi, N., Silani, V., Gellera, C., Blair, I. P., Dobson-Stone, C., Kwok, J. B., England, B. K., Bonkowski, E. S., The International ALS Genomics Consortium,, The ITALSGEN Consortium,, The FALS Sequencing Consortium,,
Source: bioRxiv
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