Amyotrophic lateral sclerosis | Current|Update|Genomics|CDC

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review.  
  Scientific reports 2017 Mar 7 44606.
  Wei QianQian, Zhou QingQing, Chen YongPing, Ou RuWei, Cao Bei, Xu YaQian, Yang Jing, Shang Hui-Fa
• Common polymorphisms of CX3CR1 gene modify ALS outcome: A population-based study.  
  Muscle & nerve 2017 Mar .
  Calvo Andrea, Moglia Cristina, Canosa Antonio, Cammarosano Stefania, Ilardi Antonio, Bertuzzo Davide, Traynor Bryan J, Brunetti Maura, Barberis Marco, Mora Gabriele, Casale Federico, Chiò Adria
• Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China.  
  Amyotrophic lateral sclerosis & frontotemporal degeneration 2017 Mar 1-4.
  Pan Chuzheng, Jiao Bin, Xiao Tingting, Hou Lihua, Zhang Weiwei, Liu Xi, Xu Jun, Tang Beisha, Shen
• CHCHD10 mutations in patients with amyotrophic lateral sclerosis in Mainland China.  
  Neurobiology of aging 2017 Feb .
  Shen Shen, He Ji, Tang Lu, Zhang Nan, Fan Dongshe
• Liver X Receptor Genes Variants Modulate ALS Phenotype.  
  Molecular neurobiology 2017 Feb .
  Mouzat Kevin, Molinari Nicolas, Kantar Jovana, Polge Anne, Corcia Philippe, Couratier Philippe, Clavelou Pierre, Juntas-Morales Raul, Pageot Nicolas, Lobaccaro Jean -Marc A, Raoul Cedric, Lumbroso Serge, Camu Willi

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