Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review.
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| Title: | Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review. |
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| Authors: | Cui F; Department of Molecular Genetics, Chifeng Maternity Hospital, Chifeng, China., Wulan T; Department of Reproduction, Chifeng Maternity Hospital, Chifeng, China., Zhang Q; AmCare Genomics Lab, Guangzhou, China., Zhang VW; AmCare Genomics Lab, Guangzhou, China., Jiang Y; Department of Obstetrics, Chifeng Maternity Hospital, Chifeng, China. |
| Source: | Frontiers in genetics [Front Genet] 2024 Mar 06; Vol. 15, pp. 1371282. Date of Electronic Publication: 2024 Mar 06 (Print Publication: 2024). |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2024.1371282 |
