A novel phenotype of 13q12.3 microdeletion characterized by epilepsy in an Asian child: a case report

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.

Source: BMC Medical Genomics - October 6, 2020 Category: Genetics & Stem Cells Authors: Mina Wang, Bin Li, Zehuan Liao, Yu Jia and Yuanbo Fu Tags: Case report Source Type: research