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Q38247539-292A5046-995F-43D5-B92A-A6E784CA6618
Q38247539-292A5046-995F-43D5-B92A-A6E784CA6618
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38247539-292A5046-995F-43D5-B92A-A6E784CA6618
Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance.
P2860
Q38247539-292A5046-995F-43D5-B92A-A6E784CA6618
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38247539-292A5046-995F-43D5-B92A-A6E784CA6618
rank
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Statement
wasDerivedFrom
b75d90bf34c56dfa58df78d8b6c9842875099c38
P2860
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome