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Q54963859-090C1ECC-2D99-4EB8-B275-661A18479C4F
Q54963859-090C1ECC-2D99-4EB8-B275-661A18479C4F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-090C1ECC-2D99-4EB8-B275-661A18479C4F
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P407
Q54963859-090C1ECC-2D99-4EB8-B275-661A18479C4F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-090C1ECC-2D99-4EB8-B275-661A18479C4F
rank
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type
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Statement
P407
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