Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy.
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| Title: | Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy. |
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| Authors: | Gong P; Department of Pediatrics, Peking University First Hospital, Beijing, China., Jiao X; Department of Pediatrics, Peking University First Hospital, Beijing, China., Yu D; Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China., Yang Z; Department of Pediatrics, Peking University First Hospital, Beijing, China. |
| Source: | Frontiers in genetics [Front Genet] 2021 Jun 30; Vol. 12, pp. 649556. Date of Electronic Publication: 2021 Jun 30 (Print Publication: 2021). |
| 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 |
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| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2021.649556 |
