Nonoda, Y., et al., Progressive diffuse brain atrophy in West syndrome with marked hypomyelination due to SPTAN1 gene mutation.Brain Dev, 2013. 35(3): p. 280-3.
Syrbe S., et al., Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy. Brain 2017; 140: 2322-2336.