Molecular investigation of TSHR gene in Bangladeshi congenital hypothyroid patients

The disorder of thyroid gland development or thyroid dysgenesis accounts for 80–85% of congenital hypothyroidism (CH) cases. Mutations in the TSHR gene are mostly associated with thyroid dysgenesis, and prevent or disrupt normal development of the gland. There is limited data available on the geneti...

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Detalles Bibliográficos
Autores principales: Begum, Mst. Noorjahan, Mahtarin, Rumana, Islam, Md. Tarikul, Ahmed, Sinthyia, Konika, Tasnia Kawsar, Mannoor, Kaiissar, Akhteruzzaman, Sharif, Qadri, Firdausi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414570/
https://www.ncbi.nlm.nih.gov/pubmed/37561783
http://dx.doi.org/10.1371/journal.pone.0282553

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414570/
https://www.ncbi.nlm.nih.gov/pubmed/37561783
http://dx.doi.org/10.1371/journal.pone.0282553

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