DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Gowda VK, Srinivasan VM, Bhat M, Benakappa A.
Case of childhood ataxia with central nervous system hypomyelination with a novel mutation in EIF2B3 gene.
J Pediatr Neurosci 2017;
12 (02) 196-198
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