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Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior
We report the genetic analysis of two consanguineous pedigrees of Pakistani ancestry in which two siblings in each family exhibited developmental delay, epilepsy, intellectual disability and aggressive behavior. Whole-genome sequencing was performed in Family 1, and we identified ~80,000 variants lo...
Autores principales: | Badshah, Noor, Mattison, Kari A., Ahmad, Sohail, Chopra, Pankaj, Johnston, H. Richard, Ahmad, Shakoor, Khan, Sher Hayat, Sarwar, Muhammad Tahir, Cutler, David J., Taylor, Micheal, Vadlamani, Gayatri, Zwick, Michael E., Escayg, Andrew |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329621/ https://www.ncbi.nlm.nih.gov/pubmed/35911904 http://dx.doi.org/10.3389/fneur.2022.918022 |
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