Predominant RET Germline Mutations in Exons 10, 11, and 16 in Iranian Patients with Hereditary Medullary Thyroid Carcinoma

Medullary thyroid carcinoma occurs in both sporadic (75%) and hereditary (25%) forms. The missense mutations of RET proto-oncogene in MTC development have been well demonstrated. To investigate the spectrum of predominant RET germline mutations in exons 10, 11, and 16 in hereditary MTC in Iranian po...

Descripción completa

Detalles Bibliográficos
Autores principales: Hedayati, Mehdi, Zarif Yeganeh, Marjan, Sheikhol Eslami, Sara, Rezghi Barez, Shekoofe, Hoghooghi Rad, Laleh, Azizi, Fereidoun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134203/
https://www.ncbi.nlm.nih.gov/pubmed/21765987
http://dx.doi.org/10.4061/2011/264248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134203/
https://www.ncbi.nlm.nih.gov/pubmed/21765987
http://dx.doi.org/10.4061/2011/264248

Ejemplares similares