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Q54963859-36B6A059-892C-4840-A190-D2B06C4C3C01
Q54963859-36B6A059-892C-4840-A190-D2B06C4C3C01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-36B6A059-892C-4840-A190-D2B06C4C3C01
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2860
Q54963859-36B6A059-892C-4840-A190-D2B06C4C3C01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-36B6A059-892C-4840-A190-D2B06C4C3C01
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2238e3b7a8168d8f852fc3ec18e83c4f39afcb1e
P2860
Reversal of Phenotypic Abnormalities by CRISPR/Cas9-Mediated Gene Correction in Huntington Disease Patient-Derived Induced Pluripotent Stem Cells.