A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: A case report

Epilepsy is a complex disorder caused by various factors, including genetic aberrance. Recent studies have identified an essential role of the sodium channel , encoded by the gene SCN8A, in epileptic encephalopathy. | A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: A case report

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