RET codon 618 mutations in Saudi families with multiple endocrine neoplasia Type 2A and familial medullary thyroid carcinoma

BACKGROUND AND OBJECTIVES: Certain diseases such as multiple endocrine neoplasia (MEN) 2A, MEN 2B, familial and sporadic medullary thyroid carcinoma (MTC) and renal dysgenesis are related to abnormalities of the RET protein. Our aim was to evaluate the frequency of RET mutation in 10 Saudi families...

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Detalles Bibliográficos
Autor principal: Qari, Faiza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078610/
https://www.ncbi.nlm.nih.gov/pubmed/23563004
http://dx.doi.org/10.5144/0256-4947.2013.155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078610/
https://www.ncbi.nlm.nih.gov/pubmed/23563004
http://dx.doi.org/10.5144/0256-4947.2013.155

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