- A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2
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Tariq H, Imran R, Naz S
- KMID: 2424178
- J Clin Neurol.
- 2018 Oct;14(4):498-504.
- doi: 10.3988/jcn.2018.14.4.498
BACKGROUND AND PURPOSE: Autosomal recessive cerebellar ataxias constitute a highly heterogeneous group of neurodegenerative disorders. This study was carried out to determine the clinical and genetic causes of ataxia in... -
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