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Q54963859-3F25B428-95F1-489F-BE59-5321B10B39BA
Q54963859-3F25B428-95F1-489F-BE59-5321B10B39BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-3F25B428-95F1-489F-BE59-5321B10B39BA
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2093
Q54963859-3F25B428-95F1-489F-BE59-5321B10B39BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-3F25B428-95F1-489F-BE59-5321B10B39BA
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P1545
11
http://www.w3.org/2001/XMLSchema#string
P2093
Samah Al-Tawalbeh
http://www.w3.org/2001/XMLSchema#string