Missense germline mutations of the RET proto-oncogene have recently been identified in the hereditary cancer syndromes MENZA, MEN2B, and FMTC, all characterized by medullary carcinoma, hut also including phaeochromocytoma in MEN2A and MEN2B and parathyroid disease in MENZA. In addition, somatic RET
✦ LIBER ✦
Mutation analysis of the RET proto-oncogene and early thyroidectomy: results of a Portuguese cancer centre
✍ Scribed by Maria João Bugalho; Rita Domingues; Jorge Rosa Santos; Ana Luísa Catarino; Luís Sobrinho
- Book ID
- 113920388
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 125 KB
- Volume
- 141
- Category
- Article
- ISSN
- 0039-6060
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