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Q54963859-0C8B7DFE-7AA0-48CC-AE56-B645CF20AD83
Q54963859-0C8B7DFE-7AA0-48CC-AE56-B645CF20AD83
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-0C8B7DFE-7AA0-48CC-AE56-B645CF20AD83
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P1433
Q54963859-0C8B7DFE-7AA0-48CC-AE56-B645CF20AD83
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-0C8B7DFE-7AA0-48CC-AE56-B645CF20AD83
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P1433
eLife