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Moreover, as multiple DNA regions can be mutated within the same gene, it is likely that the SCN1A mutation can be identified in multiple kinds of genetic epilepsies, including severe myoclonic epilepsy of infancy, epilepsy with febrile seizures plus, and partial epilepsy with febrile seizures plus
KH: Investigation, Writing original draft, Writing review & editing, Formal analysis, Validation
How quickly could a Cost Plus-type entrant access the active pharmaceutical ingredient at commercial scale
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2004;53:S1621
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