Reference database
journalVerification pending
Homozygous loss-of-function CAMK2A mutation causes growth delay, seizures and severe intellectual disability
(2018). Homozygous loss-of-function CAMK2A mutation causes growth delay, seizures and severe intellectual disability. eLife.
A verified external source link is not yet available.
Bibliography
- ID
- altawashi2018_camk2a
- PMCID
- PMC5963920
- Source-link status
- Verification pending
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