Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case–control association study reveals potential biomarkers-Reference-Cited by-同舟云学术

Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case–control association study reveals potential biomarkers

Published:2024-02-05 Issue:1 Volume:51 Page:
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Ul Mudassir Behjat,Agha Zehra

Funder

Translational Genomics Lab, COMSATS University Islamabad, Pakistan

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s11033-023-09176-9.pdf

Reference47 articles.

1. Toma C et al (2018) Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLOS Genet 14(12):e1007535. https://doi.org/10.1371/journal.pgen.1007535

2. Falsaperla R et al (2022) Intronic variant in CNTNAP2 gene in a boy with remarkable conduct disorder minor facial features mild intellectual disability and seizures. Front Pediatr. https://doi.org/10.3389/fped.2020.00550

3. Perfilyeva A, Bespalova K, Abylkassymova G, Bekmanov B, Djansugurova L (2022) rs2710102 polymorphism of the cntnap2 gene is related to autism susceptibility in a Kazakhstani population. In J Biol Chem 15(1):11–19. https://doi.org/10.26577/ijbch.2022.v15.i1.02

4. Shiota Y et al (2021) A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability. PLoS ONE 16(12):e0260548. https://doi.org/10.1371/journal.pone.0260548

5. Uddin MS et al (2021) CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case–control study combined with a meta-analysis. Hum Cell 34(5):1410–1423. https://doi.org/10.1007/s13577-021-00546-8