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Q39163038-09D27BF3-CF0D-421E-BF29-C526F5F62DD3
Q39163038-09D27BF3-CF0D-421E-BF29-C526F5F62DD3
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http://www.wikidata.org/entity/statement/Q39163038-09D27BF3-CF0D-421E-BF29-C526F5F62DD3
De novo and inherited SCN8A epilepsy mutations detected by gene panel analysis.
P2860
Q39163038-09D27BF3-CF0D-421E-BF29-C526F5F62DD3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39163038-09D27BF3-CF0D-421E-BF29-C526F5F62DD3
rank
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type
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wasDerivedFrom
91b2775af9207cba8da66af76a51ff97b63778c8
P2860
De novo mutations revealed by whole-exome sequencing are strongly associated with autism