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Q54963859-54FF0F20-2DF2-4455-9029-4264E95A6B49
Q54963859-54FF0F20-2DF2-4455-9029-4264E95A6B49
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-54FF0F20-2DF2-4455-9029-4264E95A6B49
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P1476
Q54963859-54FF0F20-2DF2-4455-9029-4264E95A6B49
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-54FF0F20-2DF2-4455-9029-4264E95A6B49
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P1476
A homozygous loss-of-function
......
severe intellectual disability
@en