Related Experiment Video
Updated: Jul 10, 2026

Rab10 Phosphorylation Detection by LRRK2 Activity Using SDS-PAGE with a Phosphate-binding Tag
Published on: December 14, 2017
Genetic aspects of restless legs syndrome
V Dhawan1, M Ali, K R Chaudhuri
1Regional Movement Disorders Unit, King's College Hospital, London, UK.
Abstract:
Restless legs syndrome (RLS), also known as Ekbom syndrome, is a common movement disorder with sensorimotor symptoms occurring during sleep and quiet wakefulness. The underlying cause for RLS is unknown but genetic influences play a strong part in the pathogenesis of RLS, particularly when the condition starts at a young age. This review explores the genetic basis of RLS and related phenotypic variations. Recently, three loci showing vulnerability to RLS have been described in French-Canadian and Italian families in chromosomes 12q, 14q and 9q, emphasising on an autosomal dominant mode of inheritance. These have been labelled RLS1, RLS2 and RLS3, respectively. However, specific causative mutations remain elusive and no linkage analysis has been identified so far in the candidate genes investigated in RLS.
Related Concept Videos
Circadian Rhythms and Gene Regulation
Human Genetics
The complex relationship between genetics and psychology is observable through common biological components such...
REM Sleep Behavior Disorder
RBD is significantly associated with...
Restless Leg Syndrome and Night Terrors
The exact cause of RLS is not fully understood, but it is believed to involve dopamine, a neurotransmitter that helps regulate muscle movement. Imbalances in dopamine levels...
Parkinson Disease l: Introduction
Alterations in Muscle Tone lll

