Case Report
Published on 08 Oct 2021
Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy
in Genetics of Common and Rare Diseases
![Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy](https://www.frontiersin.org/files/myhome article library/743833/743833_Thumb_400.jpg)
- 2,613 views
- 8 citations
Case Report
Published on 08 Oct 2021
in Genetics of Common and Rare Diseases
Clinical Trial
Published on 08 Oct 2021
in Genetics of Common and Rare Diseases
Case Report
Published on 06 Oct 2021
in Genetics of Common and Rare Diseases
Case Report
Published on 06 Oct 2021
in Genetics of Common and Rare Diseases
Case Report
Published on 05 Oct 2021
in Genetics of Common and Rare Diseases
Original Research
Published on 05 Oct 2021
in Genetics of Common and Rare Diseases
Original Research
Published on 01 Oct 2021
in Genetics of Common and Rare Diseases
Case Report
Published on 01 Oct 2021
in Genetics of Common and Rare Diseases
Correction
Published on 30 Sep 2021
in Genetics of Common and Rare Diseases
Original Research
Published on 30 Sep 2021
in Genetics of Common and Rare Diseases
Mini Review
Published on 29 Sep 2021
in Genetics of Common and Rare Diseases
Original Research
Published on 29 Sep 2021
in Genetics of Common and Rare Diseases
Brief Research Report
Published on 29 Sep 2021
in Genetics of Common and Rare Diseases
Mini Review
Published on 28 Sep 2021
in Genetics of Common and Rare Diseases
Case Report
Published on 28 Sep 2021
in Genetics of Common and Rare Diseases
Case Report
Published on 27 Sep 2021
in Genetics of Common and Rare Diseases