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H Gökce

A Family Diagnosed as MEN2A with a Rare Mutation D631Y in RET Oncogene

DOI: 
10.7727/wimj.2016.231
Synopsis: 
Mutations in the RET proto-oncogene are well documented as the genetic cause of multiple endocrine neoplasia type 2A (MEN2A) and familial medullary thyroid carcinoma (FMTC). Herein, we report a rare mutation of the RET gene (D631Y) in a Turkish family with MEN 2A.

ABSTRACT

Accepted: 
30 Jun, 2016
PDF Attachment: 
Journal Sections: 
e-Published: 19 Jul, 2016

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Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.

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