Response to Letter to the Editor: "p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer"
J Clin Endocrinol Metab
.
2018 Sep 1;103(9):3518-3519.
doi: 10.1210/jc.2018-01094.
Authors
Clare Turnbull
1
2
3
4
,
Chey Loveday
1
,
Louise Izatt
4
,
Sian Ellard
5
Affiliations
1
Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
2
William Harvey Research Institute, Queen Mary University, London, United Kingdom.
3
National Cancer Registration and Analysis Service, Public Health England, London, United Kingdom.
4
Department of Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
5
Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, United Kingdom.
PMID:
30032180
DOI:
10.1210/jc.2018-01094
No abstract available
Publication types
Letter
Comment
MeSH terms
Humans
Mutation
Proto-Oncogene Proteins c-ret / genetics
Thyroid Neoplasms*
Substances
Proto-Oncogene Proteins c-ret
RET protein, human
Grants and funding
G0700491/MRC_/Medical Research Council/United Kingdom