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: Mina Wang (Author), Bin Li (Author), Zehuan Liao (Author), Yu Jia (Author), Yuanbo Fu (Author)
Format: Book
Published: BMC, 2020-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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