Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement Disorders.

Wai Yan YauJana VandrovcovaRoisin SullivanZhongbo ChenAnna ZecchinelliRoberto CiliaStefano DugaMalgorzata MurraySusana Carmonanull nullViorica ChelbanHiroyuki IshiuraShoji TsujiZane JaunmuktaneChris TurnerNicholas W WoodHenry Houlden

Published in: Movement disorders : official journal of the Movement Disorder Society (2020)

GGC-repeat expansion in NOTCH2NLC is rare in whites presenting with movement disorders. In addition, existing whole-genome sequencing data are useful in case ascertainment. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Keyphrases

cell proliferation
risk factors
electronic health record
systematic review
machine learning
case report
big data
deep learning
meta analyses