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Q39163038-09B2F70D-98A0-4ADB-A918-4EF7697F502D
Q39163038-09B2F70D-98A0-4ADB-A918-4EF7697F502D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39163038-09B2F70D-98A0-4ADB-A918-4EF7697F502D
De novo and inherited SCN8A epilepsy mutations detected by gene panel analysis.
P2860
Q39163038-09B2F70D-98A0-4ADB-A918-4EF7697F502D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39163038-09B2F70D-98A0-4ADB-A918-4EF7697F502D
rank
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Statement
wasDerivedFrom
91b2775af9207cba8da66af76a51ff97b63778c8
P2860
Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability.