Novel Variants of <scp>IGF2</scp> Gene Are Linked With Neural Tube Defects‐An In Silico to Clinical Approach in West Bengal, India
Our research strongly suggests that genetic variations in IGF2 may help explain the risk association with NTDs and could be valuable for diagnostic and therapeutic applications.
Authors
- Susanta Sadhukhan (ORCID: https://orcid.org/0000-0002-3773-066X)
- Dinesh Munian
- Sudakshina Ghosh (ORCID: https://orcid.org/0000-0001-9393-3173)
- Madhusudan Das (ORCID: https://orcid.org/0000-0003-3748-892X)
- Srilagna Chatterjee
- Krishnendu Ghosh (ORCID: https://orcid.org/0000-0002-8423-3228)
- Biswabandhu Bankura
- Kausik Ganguly (ORCID: https://orcid.org/0000-0002-8327-0115)
- Nirvika Paul (ORCID: https://orcid.org/0000-0002-0269-6035)
- Anwesha Das (ORCID: https://orcid.org/0000-0003-4110-0297)
Institutions
- University of Calcutta (IN)
- University of Iowa (US)
- KPC Medical College and Hospital (IN)
- Vidyasagar University (IN)
- Institute of Post Graduate Medical Education and Research (IN)
Publication Details
- Journal
- Birth Defects Research
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1002/bdr2.2428
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00