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Q54963859-16D2C47E-8E41-426E-97CF-7945DEDA582E
Q54963859-16D2C47E-8E41-426E-97CF-7945DEDA582E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-16D2C47E-8E41-426E-97CF-7945DEDA582E
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2860
Q54963859-16D2C47E-8E41-426E-97CF-7945DEDA582E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-16D2C47E-8E41-426E-97CF-7945DEDA582E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2238e3b7a8168d8f852fc3ec18e83c4f39afcb1e
P2860
Genetics and the investigation of developmental delay/intellectual disability.