Genome-wide association and whole exome sequencing studies reveal a novel candidate locus for restless legs syndrome.

Ergun U., Say B., Ergun S. G., PERÇİN F. E., Inan L., Kaygisiz S., ...Daha Fazla

European journal of medical genetics, cilt.64, sa.4, ss.104186, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 64 Sayı: 4
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.ejmg.2021.104186
  • Dergi Adı: European journal of medical genetics
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, EMBASE, MEDLINE
  • Sayfa Sayıları: ss.104186
  • Anahtar Kelimeler: Restless legs syndrome, Microarray, Linkage analysis, Genome wide association, Whole exome sequencing, BINDING PROTEIN, IDENTIFICATION, EPIDEMIOLOGY, DIAGNOSIS, GENETICS
  • Gazi Üniversitesi Adresli: Evet

Özet

Introduction: The restless legs syndrome (RLS) is a common heritable neurologic disorder which is characterized by an irresistible desire to move and unpleasant sensations in the legs.