Screening of CGG Trinucleotide Repeats Within <i>FMR1</i> Gene in Bangladeshi Children With Autism Spectrum Disorder: Exploring a Possible Link With Fragile X Syndrome
This study provides preliminary evidence that CGG repeat expansion in the <i>FMR1</i> gene is unlikely to represent a major genetic contributor to ASD in Bangladeshi children. However, given the limited sample size, further investigations with a larger cohort are required to confirm these findings.
Authors
- Molie Rahman
- Mohammad Sayem (ORCID: https://orcid.org/0000-0003-0081-9457)
- Tahirah Yasmin (ORCID: https://orcid.org/0000-0002-8143-2993)
- Maisha Adiba (ORCID: https://orcid.org/0000-0002-3473-8981)
- Abdullah Al Saba (ORCID: https://orcid.org/0000-0001-6642-3952)
- A. H. M. Nurun Nabi
- Abdullah Al Noman
Institutions
- University of Dhaka (BD)
Publication Details
- Journal
- Journal of korean Academy of Child and Adolescent Psychiatry
- Published
- 2026-01-01
- DOI
- https://doi.org/10.5765/jkacap.250023
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University of Dhaka