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Q54963859-2084B178-148B-4C77-9A9B-DC3717E67C17
Q54963859-2084B178-148B-4C77-9A9B-DC3717E67C17
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Statement
http://www.wikidata.org/entity/statement/Q54963859-2084B178-148B-4C77-9A9B-DC3717E67C17
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2860
Q54963859-2084B178-148B-4C77-9A9B-DC3717E67C17
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-2084B178-148B-4C77-9A9B-DC3717E67C17
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Statement
wasDerivedFrom
2238e3b7a8168d8f852fc3ec18e83c4f39afcb1e
P2860
Temporal and region-specific requirements of αCaMKII in spatial and contextual learning.