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Article

Germline RET codon 918 mutation in apparently isolated intestinal ganglioneuromatosis.

The Journal of clinical endocrinology and metabolism - 1 Dec 1998

Eng C, Marsh D J, Robinson B G, Chow C W, Patton M A, Southey M C, Venter D J, Ponder B A, Milla P J, Smith V V

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9851750
DOI: 10.1210/jcem.83.12.5352

Genes

RET

Provenance

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

Related research

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Germline RET codon 918 mutation in apparently isolated intestinal ganglioneuromatosis.PMID 9851750Read ↗

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Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.Semantic proximity Read ↗

A novel PTEN mutation associated with colonic ganglioneuromatous polyps.Semantic proximity Read ↗

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Endothelin-3 Gene Mutations in Isolated and Syndromic Hirschsprung DiseaseSemantic proximity Read ↗

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