Severe intellectual disability, absence of language, epilepsy, microcephaly and progressive cerebellar atrophy related to the recurrent de novo variant p.(P139L) of the CAMK2B gene: A case report and brief review
| Image |  |
|---|---|
| Description | scientific article published on 01 September 2020 |
| Author/s |
author: Stefano Giuseppe Caraffi Livia Garavelli Susanna Rizzi Carlotta Spagnoli |
| Publication date | September 1, 2020 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |