Mutation Spectrum in TPO Gene of Bangladeshi Patients with Thyroid Dyshormonogenesis and Analysis of the Effects of Different Mutations on the Structural Features and Functions of TPO Protein through In Silico Approach

Although thyroid dyshormonogenesis (TDH) accounts for 10-20% of congenital hypothyroidism (CH), the molecular etiology of TDH is unknown in Bangladesh. Thyroid peroxidase (TPO) is most frequently associated with TDH and the present study investigated the spectrum of TPO mutations in Bangladeshi pati...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Biomed Res Int
Autores principales: Begum, Mst. Noorjahan, Islam, Md Tarikul, Hossain, Shekh Rezwan, Bhuyan, Golam Sarower, Halim, Mohammad A., Shahriar, Imrul, Sarker, Suprovath Kumar, Haque, Shahinur, Konika, Tasnia Kawsar, Islam, Md. Sazzadul, Rahat, Asifuzzaman, Qadri, Syeda Kashfi, Sultana, Rosy, Begum, Suraiya, Sultana, Sadia, Saha, Narayan, Hasan, Mizanul, Hasanat, M. A., Banu, Hurjahan, Shekhar, Hossain Uddin, Chowdhury, Emran Kabir, Sajib, Abu A., Islam, Abul B. M. M. K., Qadri, Syed Saleheen, Qadri, Firdausi, Akhteruzzaman, Sharif, Mannoor, Kaiissar
Formato: Artigo
Lenguaje:Inglês
Publicado: Hindawi 2019
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6409061/
https://ncbi.nlm.nih.gov/pubmed/30915365
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/9218903
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares