Case report: A novel de novo variant of NACC1 caused epileptic encephalopathy and intellectual disability
BackgroundGenetic disorders could also contribute to intellectual disability. Using whole exome sequencing (WES), several variants have been identified as autosomal-dominant inheritance intellectual disability. Thus, the application of WES has demonstrated its critical role in distinguishing intelle...
সংরক্ষণ করুন:
| প্রধান লেখক: | , , , , |
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| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
Frontiers Media S.A.
2024-10-01
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| মালা: | Frontiers in Psychiatry |
| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://www.frontiersin.org/articles/10.3389/fpsyt.2024.1446698/full |
| ট্যাগগুলো: |
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