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Q54963859-A141E68B-8765-4FA6-AE42-84288EFEB950
Q54963859-A141E68B-8765-4FA6-AE42-84288EFEB950
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-A141E68B-8765-4FA6-AE42-84288EFEB950
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P50
Q54963859-A141E68B-8765-4FA6-AE42-84288EFEB950
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-A141E68B-8765-4FA6-AE42-84288EFEB950
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P1545
3
http://www.w3.org/2001/XMLSchema#string
P50
Shinsuke Niwa