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Article

RET oncogene.

Current opinion in genetics & development - 1 Feb 1996

Mak Y F, Ponder B A

Abstract excerpt

RET mutations have been identified as the underlying cause of two congenital diseases that predominately affect tissues of neural crest origin: the MEN 2 cancer syndromes and a proportion of cases of dominantly inherited Hirschsprung disease, a disorder of gut development. This review summarizes...

Topics

Animals
Drosophila Proteins
Hirschsprung Disease
Humans
Multiple Endocrine Neoplasia Type 2a
Mutation
Phenotype
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-ret
Receptor Protein-Tyrosine Kinases

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8791480
DOI: 10.1016/s0959-437x(96)90015-5

Genes

RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8791480-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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