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Q39163038-00144EE6-D8ED-43F6-A1A0-5A398AEC9FA1
Q39163038-00144EE6-D8ED-43F6-A1A0-5A398AEC9FA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39163038-00144EE6-D8ED-43F6-A1A0-5A398AEC9FA1
De novo and inherited SCN8A epilepsy mutations detected by gene panel analysis.
P2860
Q39163038-00144EE6-D8ED-43F6-A1A0-5A398AEC9FA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39163038-00144EE6-D8ED-43F6-A1A0-5A398AEC9FA1
rank
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Statement
wasDerivedFrom
91b2775af9207cba8da66af76a51ff97b63778c8
P2860
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy