Germline RET V804M mutation associated with multiple endocrine neoplasia type 2A
- 2 August 2004
- journal article
- case report
- Published by Oxford University Press (OUP) in British Journal of Surgery
- Vol. 91 (11) , 1458-1459
- https://doi.org/10.1002/bjs.4718
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- V804M RET mutation and familial medullary thyroid carcinoma: Report of a large family with expression of the disease only in the homozygous gene carriersSurgery, 2002
- Familial medullary thyroid carcinoma and prominent corneal nerves associated with the germline V804M and V778I mutations on the same allele of RETJournal of Medical Genetics, 2001
- Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG→ATG) mutationSurgery, 2000
- Two Germline Missense Mutations at Codons 804 and 806 of the RET Proto‐oncogene in the Same Allele in a Patient with Multiple Endocrine Neoplasia Type 2B without Codon 918 MutationJapanese Journal of Cancer Research, 1999
- The Relationship Between Specific RET Proto-oncogene Mutations and Disease Phenotype in Multiple Endocrine Neoplasia Type 2JAMA, 1996
- Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of theRET proto-oncogeneInternational Journal of Cancer, 1996