Screening of novel restless legs syndrome–associated genes in French-Canadian families

Lignende værker

• SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome
  af: Sarayloo, Faezeh, et al.
  Udgivet: (2020)
• Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum
  af: Noreau, Anne, et al.
  Udgivet: (2014)
• Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population
  af: Zhou, Sirui, et al.
  Udgivet: (2018)
• Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression
  af: Sarayloo, Faezeh, et al.
  Udgivet: (2019)
• Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes
  af: Akçimen, Fulya, et al.
  Udgivet: (2020)