DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Xu X, Yang X, Wu Q. et al.
Amplicon resequencing identified parental mosaicism for approximately 10% of “de novo” SCN1A mutations in children with Dravet syndrome.
Hum Mutat 2015;
36 (09) 861-872
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