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Journal: GenesVolume: 14Number: 1177
Article: CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report
- Authors:
- Ekaterina R. Tolmacheva,
- Jekaterina Shubina and
- Taisiya O. Kochetkova
- et al.
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