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Polymorphic Variants of FOXP3 Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India) Cover

Polymorphic Variants of FOXP3 Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India)

Journal of Mother and Child
Volume 29 (2025): Issue 1 (February 2025)
By: Usma Manzoor,  Arshad A. Pandith,  Tawseef A. Lone,  Amreena Hameed,  Falak U Nisa,  Ina Amin,  Shayesta Rah,  Saima Wani,  Shayaq Ul Abeer Rasool,  Adil Lateef and  Aabida Ahmad  
Open Access
|Dec 2025

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DOI: https://doi.org/10.34763/jmotherandchild.20252901.d-25-00030 | Journal eISSN: 2719-535X | Journal ISSN: 2719-6488
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Language: English
Page range: 219 - 226
Submitted on: Aug 11, 2025
Accepted on: Sep 12, 2025
Published on: Dec 4, 2025
Published by: Institute of Mother and Child
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
Keywords:
FOXP3,
Recurrent Pregnancy Loss,
Polymorphic Variations,
Treg cells,
Genotyping
Related subjects:
Medicine,
Clinical medicine,
Pediatrics and juvenile medicine,
Paediatric haematology and oncology,
Public health

© 2025 Usma Manzoor, Arshad A. Pandith, Tawseef A. Lone, Amreena Hameed, Falak U Nisa, Ina Amin, Shayesta Rah, Saima Wani, Shayaq Ul Abeer Rasool, Adil Lateef, Aabida Ahmad, published by Institute of Mother and Child
This work is licensed under the Creative Commons Attribution 4.0 License.

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