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Recently, p.R383H in TFG was identified as the disease cause in a family with α‐synucleinopathy and amyotrophic lateral sclerosis (ALS). However, no further replication has been conducted in larger cohorts. Click to show full abstract
Recently, p.R383H in TFG was identified as the disease cause in a family with α‐synucleinopathy and amyotrophic lateral sclerosis (ALS). However, no further replication has been conducted in larger cohorts.
Keywords:
mutation screening;
synucleinopathy amyotrophic;
lateral sclerosis;
tfg;
amyotrophic lateral
Journal Title: Movement Disorders
Year Published: 2022
Link to full text (if available)
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Journal Title: Movement Disorders
Year Published: 2022
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!