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Q54963859-031A4749-9AAE-47B4-8E55-D42529F98388
Q54963859-031A4749-9AAE-47B4-8E55-D42529F98388
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-031A4749-9AAE-47B4-8E55-D42529F98388
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P31
Q54963859-031A4749-9AAE-47B4-8E55-D42529F98388
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-031A4749-9AAE-47B4-8E55-D42529F98388
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P31
scholarly article