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Article

The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case.

Surgery - 1 May 2005

Aiello Antonella, Cioni Katia, Gobbo Morena, Collini Paola, Gullo Maria, Della Torre Gabriella, Passerini Emanuele, Ferrando Barbara, Pilotti Silvana, Pierotti Marco A, Pasini Barbara

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15855933
DOI: 10.1016/j.surg.2005.01.014

Genes

RET

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case.PMID 15855933Read ↗

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Germline Dinucleotide Mutation in Codon 883 of the<i>RET</i>Proto-Oncogene in Multiple Endocrine Neoplasia Type 2B Without Codon 918 MutationSemantic proximity Read ↗

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