Whole Exome Sequencing in Intellectual Disability Patients Identifies de novo Mutations in KCNB1, SHANK2, and SYNGAP1 Genes and a Novel Mutation in PPP1R3F.
| Autor: | Alkhateeb, Asem M.1 asemalkhateeb@just.edu.jo, Almomani, Miral2, Hammad, Hani H.1 |
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| Zdroj: | Jordan Journal of Biological Sciences. Dec2023, Vol. 16 Issue 4, p593-597. 5p. |
| Databáze: | Academic Search Ultimate |
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