DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Cheng Y, Zhang L, Huang X. et al.
De novo SCN2A mutation in a Chinese infant with severe early-onset epileptic encephalopathy, bronchopulmonary dysplasia, and adrenal hypofunction.
Int J Clin Exp Pathol 2017;
10 (10) 10358-10362
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