An Overview of UBTF Neuroregression Syndrome
Recently, a recurrent de novo dominant mutation in <i>UBTF</i> (c.628G>A, p.Glu210Lys; <i>UBTF</i> E210K) was identified as the cause of a neurological disorder which has been named UBTF Neuroregression Syndrome (UNS), or Childhood-Onset Neurodegeneration with Brain Atroph...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2024-02-01
|
Series: | Brain Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/2076-3425/14/2/179 |