Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit
-
Published:2023-10-17
Issue:6
Volume:12
Page:1821-1843
-
ISSN:2193-8253
-
Container-title:Neurology and Therapy
-
language:en
-
Short-container-title:Neurol Ther
Author:
Sattler RitaORCID, Traynor Bryan J.ORCID, Robertson JaniceORCID, Van Den Bosch LudoORCID, Barmada Sami J.ORCID, Svendsen Clive N.ORCID, Disney Matthew D.ORCID, Gendron Tania F.ORCID, Wong Philip C.ORCID, Turner Martin R.ORCID, Boxer AdamORCID, Babu SumaORCID, Benatar MichaelORCID, Kurnellas MichaelORCID, Rohrer Jonathan D.ORCID, Donnelly Christopher J.ORCID, Bustos Lynette M., Van Keuren-Jensen Kendall, Dacks Penny A., Sabbagh Marwan N.ORCID, Alessandrini Francesco, Andrews Jinsy A., Bakkar Nadine, Berry James D., Boeve Brad F., Bowser Robert, Burke Anna D., Cridebring Derek, Cummings Jeffrey L., Ejebe Kenechi G., Gittings Lauren M., Gao Fen-Biao, Haeusler Aaron R., Ichida Justin K., Jafar-Nejad Paymaan, Kinney Jefferson W., Ladha Shafeeq S., Lewcock Joseph W., Linerud Joanne L., Medina David X., Niehoff Debra L., Nilsson Mark, Nilsson Paula, Penner Cooper, Rothstein Jeffrey D., Satlin Andrew, Scannevin Robert H., Shefner Jeremy M., Shin Hijai Regina, Staffaroni Adam M., Sun Shuying, Thakur Neil M., Vieira Fernando G.,
Funder
Barrow Neurological Foundation National Institute on Aging Arizona Community Foundation
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference130 articles.
1. Grassano M, Calvo A, Moglia C, Sbaiz L, Brunetti M, Barberis M, et al. Systematic evaluation of genetic mutations in ALS: a population-based study. J Neurol Neurosurg Psychiatry. 2022;93(11):1190–3. 2. Kirola L, Mukherjee A, Mutsuddi M. Recent updates on the genetics of amyotrophic lateral sclerosis and frontotemporal dementia. Mol Neurobiol. 2022;59(9):5673–94. 3. Laaksovirta H, Peuralinna T, Schymick JC, Scholz SW, Lai SL, Myllykangas L, et al. Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. Lancet Neurol. 2010;9(10):978–85. 4. Renton AE, Majounie E, Waite A, Simon-Sanchez J, Rollinson S, Gibbs JR, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron. 2011;72(2):257–68. 5. Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, et al. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol. 2012;11(4):323–30.
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
|
|