Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India.
Saved in:
| Title: | Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India. |
|---|---|
| Authors: | Shah, Jhanvi1 (AUTHOR), Mondal, Debasrija2 (AUTHOR), Jain, Deepika3 (AUTHOR), Mhatre, Priti4 (AUTHOR), Patel, Ketan5 (AUTHOR), Iyer, Anand6 (AUTHOR), Pandya, Manoj7 (AUTHOR), Menghani, Bhargavi8 (AUTHOR), Dave, Gayatri9 (AUTHOR), Sheth, Jayesh1 (AUTHOR), Sheth, Frenny1 (AUTHOR), Ramdas, Shweta2 (AUTHOR) shwetaramdas@iisc.ac.in, Sheth, Harsh1 (AUTHOR) harsh.sheth@frige.co.in |
| Source: | BMC Medical Genomics. 8/20/2025, Vol. 18 Issue 1, p1-12. 12p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 17558794 |
|---|---|
| DOI: | 10.1186/s12920-025-02204-6 |
