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Article

RET mutations in multiple endocrine neoplasia type 2 and Hirschsprung disease.

Current opinion in pediatrics - 1 Dec 1995

Reynolds L F, Eng C

Abstract excerpt

Mutations in the RET proto-oncogene have been found in a large proportion of families affected by the multiple endocrine neoplasia type 2 syndrome and in familial and sporadic Hirschsprung disease. This review discusses the role of the RET receptor tyrosine kinase in the etiology of these dominantly inherited disorders of neural crest development. In addition, the role of genetic screening is considered in the...

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Source

Identifiers

PMID: 8776023
DOI: 10.1097/00008480-199512000-00014

Genes

RET

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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