DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

References

Darras N, Ha TK, Rego S. et al.
Developmental and epileptic encephalopathy in two siblings with a novel, homozygous missense variant in SCN1B.

Am J Med Genet A 2019;
179 (11) 2190-2195

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