One hundred and seven member family with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: Is this a new syndrome–MEN 2C?

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Bibliographische Detailangaben
Veröffentlicht in:	Surgery 2010-09, Vol.148 (3), p.611-612
Hauptverfasser:	Shifrin, Alexander L., MD, FACS, Fay, Angela M., MS, CGC, Xenachis, Cristina Z., MD, Vernick, Jerome J., MD, FACS
Format:	Artikel
Sprache:	eng
Schlagworte:	Gene Rearrangement - genetics Humans Hyperparathyroidism - complications Hyperparathyroidism - genetics Multiple Endocrine Neoplasia Type 2a - genetics Pheochromocytoma - genetics Proto-Oncogenes - genetics Surgery Syndrome Thyroid Neoplasms - complications Thyroid Neoplasms - genetics
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