Article
Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
Thyroid : official journal of the American Thyroid Association - 1 Dec 2017
Lebeault Maylis, Pinson Stéphane, Guillaud-Bataille Marine, Gimenez-Roqueplo Anne-Paule, Carrie Alain, Barbu Véronique, Pigny Pascal, Bezieau Stéphane, Rey Jean-Marc, Delvincourt Chantal, Giraud Sophie, Veyrat-Durebex Charlotte, Saulnier Patrick, Bouzamondo Nathalie, Chabbert Marie, Blin Julien, Mohamed Amira, Romanet Pauline, Borson-Chazot Francoise, Rohmer Vincent, Barlier Anne, Mirebeau-Prunier Delphine
Abstract excerpt
BACKGROUND: The presence of single nucleotide polymorphisms (SNPs) in the REarranged during Transfection (RET) gene has been investigated with regard to their potential role in the development or progression of medullary thyroid cancer or pheochromocytomas (PHEO) in patients with the multiple endocrine neoplasia type 2 (MEN2) syndrome. The aim of this study was to evaluate the spectrum of RET variants in France...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
