DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Henriksen MW, Ravn K, Paus B, von Tetzchner S, Skjeldal OH.
De novo mutations in SCN1A are associated with classic Rett syndrome: a case report.
BMC Med Genet 2018;
19 (01) 184
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