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Article

A Novel Missense Mutation in the MEN1 Gene in A Patient with Multiple Endocrine Neoplasia type 1

31 Mar 2011

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 21454242
DOI: 10.4158/ep10291.cr

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Related research

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Research trail→

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A Novel Missense Mutation in the MEN1 Gene in A Patient with Multiple Endocrine Neoplasia type 1PMID 21454242Read ↗

A new mutation in the MEN1 gene.Semantic proximity Read ↗

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

A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine neoplasia-type 1 (MEN1).Semantic proximity Read ↗

A patient with multiple endocrine neoplasia type 1 with a novel MEN1 gene mutation (237delC).Semantic proximity Read ↗

The MEN1 gene and associated diseases: an update.Semantic proximity Read ↗

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseasesSemantic proximity Read ↗

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the geneSemantic proximity Read ↗

Identification of Novel Variants in MEN1: A Study Conducted with Four Multiple Endocrine Neoplasia Type 1 Patients.Semantic proximity Read ↗

Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine yearsSemantic proximity Read ↗

Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database.Semantic proximity Read ↗

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related statesSemantic proximity Read ↗

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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