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PubMed (OMIM) for id: 26039

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Genetic analysis of SS18L1 in French amyotrophic lateral sclerosis.
Teyssou E, Vandenberghe N, Moigneu C, Boillée S, Couratier P, Meininger V, Pradat PF, Salachas F, Leguern E, Millecamps S. Teyssou E, et al. Neurobiol Aging. 2014 May;35(5):1213.e9-1213.e12. doi: 10.1016/j.neurobiolaging.2013.11.023. Epub 2013 Dec 3. Neurobiol Aging. 2014. PMID: 24360741
Exome sequencing to identify de novo mutations in sporadic ALS trios.
Chesi A, Staahl BT, Jovičić A, Couthouis J, Fasolino M, Raphael AR, Yamazaki T, Elias L, Polak M, Kelly C, Williams KL, Fifita JA, Maragakis NJ, Nicholson GA, King OD, Reed R, Crabtree GR, Blair IP, Glass JD, Gitler AD. Chesi A, et al. Nat Neurosci. 2013 Jul;16(7):851-5. doi: 10.1038/nn.3412. Epub 2013 May 26. Nat Neurosci. 2013. PMID: 23708140 Free PMC article.