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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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King Faisal Specialist Hospital and Research Centre
2013
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| 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 |