[Epilepsy and other phenotypic features of X-linked intellectual disability caused by the mutations in the KIAA2022 gene].
- DOI
- 10.17116/jnevro202212209214
- Published
- 2022
- Container
- Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.17116/jnevro202212209214,
title = {[Epilepsy and other phenotypic features of X-linked intellectual disability caused by the mutations in the KIAA2022 gene].},
author = {Gamirova RG and Barkov AI and Shaimuchametova VA and Liukshina NG and Volkov IV and Tomenko TR and Rachmanina OA and Shestakova OI and Gorobets EA},
year = {2022},
journal = {Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova},
doi = {10.17116/jnevro202212209214},
url = {https://doi.org/10.17116/jnevro202212209214}
}RIS
TY - JOUR TI - [Epilepsy and other phenotypic features of X-linked intellectual disability caused by the mutations in the KIAA2022 gene]. AU - Gamirova RG AU - Barkov AI AU - Shaimuchametova VA AU - Liukshina NG AU - Volkov IV AU - Tomenko TR AU - Rachmanina OA AU - Shestakova OI AU - Gorobets EA PY - 2022 JO - Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova DO - 10.17116/jnevro202212209214 UR - https://doi.org/10.17116/jnevro202212209214 ER -
APA
RG, G., AI, B., VA, S., NG, L., IV, V., TR, T., OA, R., OI, S., & EA, G. (2022). [Epilepsy and other phenotypic features of X-linked intellectual disability caused by the mutations in the KIAA2022 gene].. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. https://doi.org/10.17116/jnevro202212209214
Source records
- pubmed · retrieved 2026-09-26T14:15:03.025Z