Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma-Reference-Cited by-同舟云学术

Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma

Published:2011-11-09 Issue:1 Volume:11 Page:131-136
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Qi X.-P.,Ying R.-B.,Ma J.-M.,Liu W.-T.,Du Z.-F.,Fei J.,Yang C.-P.,Song Q.-Z.,Jin H.-Y.,Chen Z.-G.,Han J.-S.,Wang J.-Q.,Chen X.-L.,Zhao Y.,Lu J.-J.,Zhang X.-N.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-011-9487-1.pdf

Reference23 articles.

1. Kloos RT, Eng C et al (2009) Medullary thyroid cancer: management guidelines of the American Thyroid Association. Thyroid 19:565–612

2. Qi XP, Ma JM et al (2011) RET germline mutations identified by exome sequencing in a Chinese multiple endocrine neoplasia type 2A/familial medullary thyroid carcinoma family. Plos One 6:e20353

3. Eng C, Clayton D et al (1996) The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. JAMA 276:1575–1579

4. Raue F, Frank-Raue K (2010) Update multiple endocrine neoplasia type 2. Fam Cancer 9:449–457

5. Frank-Raue K, Rondot S, Raue F (2010) Molecular genetics and phenomics of RET mutations: impact on prognosis of MTC. Mol Cell Endocrinol 322:2–7

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1. Multiple Endocrine Neoplasia Type 2B Associated Mixed Medullary and Follicular Thyroid Carcinoma in A Chinese Patient with RET M918T Germline Mutation;Endocrine, Metabolic & Immune Disorders - Drug Targets;2021-03

2. 5P Strategies for Management of Multiple Endocrine Neoplasia Type 2: A Paradigm of Precision Medicine;Frontiers in Endocrinology;2020-09-18

3. Unique association of multiple endocrine neoplasia 2A and congenital anomalies of the kidney and urinary tract in a child with a RET mutation;BMJ Case Reports;2019-08

4. Letter to the Editor regarding the paper by N. Azzam et al. ‘Germline polymorphisms on RET proto-oncogene involved in medullary thyroid carcinoma in a Druze family’;European Journal of Cancer;2018-04

5. Clinical significance of RET mutation screening in a pedigree of multiple endocrine neoplasia type 2A;Molecular Medicine Reports;2016-06-06