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Q54963859-D540195E-927D-4687-B879-5594DAB2FE74
Q54963859-D540195E-927D-4687-B879-5594DAB2FE74
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-D540195E-927D-4687-B879-5594DAB2FE74
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P478
Q54963859-D540195E-927D-4687-B879-5594DAB2FE74
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-D540195E-927D-4687-B879-5594DAB2FE74
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P478
7
http://www.w3.org/2001/XMLSchema#string