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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...

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Detalhes bibliográficos
Main Authors: Mehdi Hedayati, Marjan Zarif Yeganeh, Sara Sheikhol Eslami, Shekoofe Rezghi Barez, Laleh Hoghooghi Rad, Fereidoun Azizi
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Limited 2011-01-01
Colecção:Journal of Thyroid Research
Acesso em linha:http://dx.doi.org/10.4061/2011/264248
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