A novel phenotype of 13q12.3 microdeletion characterized by epilepsy in an Asian child: a case report
Abstract Background The microdeletion of chromosome 13 has been rarely reported. Here, we report a 14-year old Asian female with a de novo microdeletion on 13q12.3. Case presentation The child suffered mainly from two types of epileptic seizures: partial onset seizures and myoclonic seizures, accomp...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
BMC,
2020-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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