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Mutated SCN1A decreases the amount of pyraclofos. 1 / 1

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"Dravet syndrome is a severe infant-onset epileptic encephalopathy most often caused by de novo mutation of SCN1A resulting in heterozygous loss-of-function of the Nav1.1 voltage gated sodium channel 1."

29127345

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IndraLab

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Mutated SCN1A decreases the amount of pyraclofos. 1 / 1

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