The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case.

Aiello, Antonella

The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case. [electronic resource] - Surgery May 2005 - 574-6 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0039-6060

10.1016/j.surg.2005.01.014 doi


Carcinoma--genetics
Female
Humans
Middle Aged
Multiple Endocrine Neoplasia Type 2a--genetics
Mutation--genetics
Oncogene Proteins--genetics
Proto-Oncogene Proteins c-ret
Receptor Protein-Tyrosine Kinases--genetics
Thyroid Neoplasms--genetics