Article
A Novel TFG Mutation in a Korean Family with α-Synucleinopathy and Amyotrophic Lateral Sclerosis.
Movement disorders : official journal of the Movement Disorder Society - 1 Feb 2022
Yoo Dallah, Lee Wonjae, Lee Seung-Jae, Sung Jung-Joon, Jeon Gye Sun, Ban Jae-Jun, Shin Chaewon, Kim Jungho, Kim Hyo Sun, Ahn Tae-Beom
Abstract excerpt
BACKGROUND: Tropomyosin-receptor kinase fused gene (TFG) functions as a regulator of intracellular protein packaging and trafficking at the endoplasmic reticulum exit sites. TFG has recently been proposed as a cause of multisystem proteinopathy. OBJECTIVES: Here, we describe a Korean family presenting with Parkinson's disease or amyotrophic lateral sclerosis caused by a novel variant of TFG (c.1148 G > A,...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
