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

ERGÜN, UFUK; Say, Bahar; Ergun, SEZEN; PERÇİN, FERDA; Inan, Levent; Kaygisiz, Sukran; Asal, Pinar; Yurteri, Buket; Struchalin, Maksim; Shtokalo, Dmitry; ERGÜN, MEHMET

doi:10.1016/j.ejmg.2021.104186

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, Scopus)

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.