A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
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| Description | scientific article |
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author: Mahmoud A. Pouladi Shinsuke Niwa Franklin L Zhong Stanley F Nelson Poh Hui Chia Bruno Reversade |
| Publication date | May 22, 2018 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |