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Published in 2022 at "Movement Disorders"
DOI: 10.1002/mds.29079
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.
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Keywords:
mutation screening;
synucleinopathy amyotrophic;
lateral sclerosis;
tfg ... See more keywords