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Article

Five novel mutations in the familial multiple endocrine neoplasia type 1 (MEN1) gene. Mutations in brief no. 188. Online.

Human mutation - 1 Jan 1998

Cote G J, Lee J E, Evans D B, Huang E, Schultz P N, Dang G T, Qiu H, Shetelbine S, Sellin R V, Gagel R F

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 10660339

Genes

MEN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Five novel mutations in the familial multiple endocrine neoplasia type 1 (MEN1) gene. Mutations in brief no. 188. Online.PMID 10660339Read ↗

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Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: Additional information for mutational screening.Semantic proximity Read ↗

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Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)Semantic proximity Read ↗

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