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RACGAP1 variants in a sporadic case of CDA III implicates the dysfunction of centralspindlin as the basis of the disease.

Sandeep N WontakalMishan BrittoHuan ZhangYongshuai HanChengjie GaoSarah TannenbaumBenjamin H DurhamMargaret T LeeXiuli AnMasanori Mishima
Published in: Blood (2021)
Keyphrases
  • copy number
  • late onset
  • oxidative stress
  • amyotrophic lateral sclerosis
  • gene expression
  • early onset
  • genome wide