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Q54963859-CFAB80BD-D5AA-4B3F-9B71-B1C738E46C10
Q54963859-CFAB80BD-D5AA-4B3F-9B71-B1C738E46C10
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-CFAB80BD-D5AA-4B3F-9B71-B1C738E46C10
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P698
Q54963859-CFAB80BD-D5AA-4B3F-9B71-B1C738E46C10
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-CFAB80BD-D5AA-4B3F-9B71-B1C738E46C10
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P698
29784083
http://www.w3.org/2001/XMLSchema#string