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


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

EUROPEAN JOURNAL OF MEDICAL GENETICS, cilt.64, sa.4, 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
  • Hacettepe 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.