De novo homozygous variant of the SCN1A gene in a patient with severe Dravet syndrome complicated by acute encephalopathy.
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| Title: | De novo homozygous variant of the SCN1A gene in a patient with severe Dravet syndrome complicated by acute encephalopathy. |
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| Authors: | Van LTK; Neurology Department, Children Hospital 2, Ho Chi Minh City, 70000, Vietnam., Hien HTD; Research Center for Genetics and Reproductive Health, School of Medicine, Vietnam National University HCMC, Ho Chi Minh City, 70000, Vietnam., Kieu HTT; Neurology Department, Children Hospital 2, Ho Chi Minh City, 70000, Vietnam., Hieu NLT; Neurology Department, Children Hospital 2, Ho Chi Minh City, 70000, Vietnam., Vinh LS; University of Engineering and Technology, Vietnam National University Hanoi, Hanoi, 10000, Vietnam., Hoa G; Medical Genetics Institute, Ho Chi Minh City, 70000, Vietnam., Hang DTT; Research Center for Genetics and Reproductive Health, School of Medicine, Vietnam National University HCMC, Ho Chi Minh City, 70000, Vietnam. dtthang@medvnu.edu.vn. |
| Source: | Neurogenetics [Neurogenetics] 2021 May; Vol. 22 (2), pp. 133-136. Date of Electronic Publication: 2021 Mar 05. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1364-6753 (Electronic) Linking ISSN: 13646745 NLM ISO Abbreviation: Neurogenetics Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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