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Q54963859-1F211B1F-1392-439E-A72A-BB375EBDDD05
Q54963859-1F211B1F-1392-439E-A72A-BB375EBDDD05
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-1F211B1F-1392-439E-A72A-BB375EBDDD05
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2860
Q54963859-1F211B1F-1392-439E-A72A-BB375EBDDD05
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-1F211B1F-1392-439E-A72A-BB375EBDDD05
rank
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type
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wasDerivedFrom
2238e3b7a8168d8f852fc3ec18e83c4f39afcb1e
P2860
Neuronal CA2+/calmodulin-dependent protein kinase II: the role of structure and autoregulation in cellular function