Persistent URL of this record https://hdl.handle.net/1887/3251143
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Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis
- All authors
- Johnson, J.O.; Chia, R.; Miller, D.E.; Li, R.; Kumaran, R.; Abramzon, Y.; Alahmady, N.; Renton, A.E.; Topp, S.D.; Gibbs, J.R.; Cookson, M.R.; Sabir, M.S.; Dalgard, C.L.; Troakes, C.; Jones, A.R.; Shatunov, A.; Iacoangeli, A.; Khleifat, A. al; Ticozzi, N.; Silani, V.; Gellera, C.; Blair, I.P.; Dobson-Stone, C.; Kwok, J.B.; Bonkowski, E.S.; Palvadeau, R.; Tienari, P.J.; Morrison, K.E.; Shaw, P.J.; Al-Chalabi, A.; Jr, R.H.B.; Calvo, A.; Mora, G.; Al-Saif, H.; Gotkine, M.; Leigh, F.; Chang, I.J.; Perlman, S.J.; Glass, I.; Scott, A.I.; Shaw, C.E.; Basak, A.N.; Landers, J.E.; Chio, A.; Crawford, T.O.; Smith, B.N.; Traynor, B.J.; FALS Sequencing Consortium; Amer Genome Ctr; Int ALS Genomics Consortium; ITALSGEN Consortium
- Date
- 2021-08-30
- Journal
- JAMA Neurology
- Volume
- 78
- Issue
- 10
- Pages
- 1236 - 1248