Truncating mutation in TANC2 in a Chinese boy associated with Lennox-Gastaut syndrome: a case report
Abstract Background Lennox-Gastaut syndrome (LGS) is a severe epileptic encephalopathy that can be caused by brain malformations or genetic mutations. Recently, genome-wide association studies have led to the identification of novel mutations associated with LGS. The TANC2 gene, encodes a synaptic s...
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| Auteurs principaux: | , , , , , , , |
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| Format: | article |
| Langue: | EN |
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BMC
2021
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| Accès en ligne: | https://doaj.org/article/c41c125a66124044a264135caf58bafd |
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