V804M RET mutation and familial medullary thyroid carcinoma: Report of a large family with expression of the disease only in the homozygous gene carriers-Reference-Cited by-同舟云学术

V804M RET mutation and familial medullary thyroid carcinoma: Report of a large family with expression of the disease only in the homozygous gene carriers

Published:2002-05 Issue:5 Volume:131 Page:509-514
ISSN:0039-6060
Container-title:Surgery
language:en
Short-container-title:Surgery

Author:

Lecube Albert,Hernandez Cristina,Oriola Josep,Galard Rosa,Gémar Enrique,Mesa Jorge,Simó Rafael

Publisher

Elsevier BV

Subject

Surgery

Reference27 articles.

1. Analysis of RET proto-oncogene point mutations distinguishes heritable from non-heritable medullary thyroid carcinomas;Komminoth;Cancer,1995

2. RET receptor tyrosine kinase gene mutations: molecular biological, physiological and clinical aspects;Hoppener;Eur J Clin Invest,1996

3. Specific mutation of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC;Mulligan;Nat Genet,1994

4. Genotype-phenotype correlation in MEN type 2: report of the International RET Mutation Consortium;Mulligan;J Intern Med,1995

5. The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2;Eng;JAMA,1996

Cited by 41 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Accelerated MEN2A in homozygous RET carriers in the context of consanguinity;European Journal of Endocrinology;2024-03

2. The Pathogenic RET Val804Met Variant in Acromegaly: A New Clinical Phenotype?;International Journal of Molecular Sciences;2024-02-05

3. Discussion;Surgery;2023-01

4. Medullary thyroid cancer with RET V804M mutation: more indolent than expected?;Surgery;2023-01

5. Multiple endocrine neoplasia type 2 (MEN2) and RET specific modifications of the ACMG/AMP variant classification guidelines and impact on the MEN2 RET database;Human Mutation;2022-10-31