Associated Papers
Double mutation for multiple endocrine neoplasia associated with congenital adrenal hyperplasia.
de Oliveira WL et al.
Endocrinology, Diabetes & Metabolism Case Reports, 2025
Characterization of the Thyroid Cancer Genomic Landscape by Plasma-Based Circulating Tumor DNA Next-Generation Sequencing.
Tarasova VD et al.
Thyroid : Official Journal of the American Thyroid Association, 2024
GLOBAL ENDOCRINOLOGY: Geographical variation in the profile of RET variants in patients with medullary thyroid cancer: a comprehensive review.
Maciel RMB et al.
European Journal of Endocrinology, 2021
A Homozygous RET K666N Genotype With an MEN2A Phenotype.
Jaber T et al.
The Journal of Clinical Endocrinology and Metabolism, 2018
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
Xu JY et al.
Thyroid : Official Journal of the American Thyroid Association, 2016
A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma.
Yamazaki M et al.
Endocrine Journal, 2014
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