SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures
Abstract Background SCN8A mutations have recently been associated with epilepsy and neurodevelopmental disorders. This study aimed to broaden the phenotypic-spectrum of disease related with SCN8A mutations. Methods To identify the pathogenic gene of a Chinese family, in which six members suffered fr...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2017-09-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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