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Article

MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?

The British journal of dermatology - 1 Jan 2007

Mangold E, Rahner N, Friedrichs N, Buettner R, Pagenstecher C, Aretz S, Friedl W, Ruzicka T, Propping P, Rütten A, Kruse R

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Source

Identifiers

PMID: 17199584
DOI: 10.1111/j.1365-2133.2006.07607.x

Genes

MSH6

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

Related research

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Research trail→

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New mutation in the hMSH2 gene in a Spanish Muir-Torre syndrome.Semantic proximity Read ↗

Muir-Torre syndrome: Diagnostic and screening guidelines.Semantic proximity Read ↗

Spectrum of genetic alterations in Muir‐Torre syndrome is the same as in HNPCCSemantic proximity Read ↗

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents.Semantic proximity Read ↗

A Homozygous MSH6 Mutation in a Child with Café-au-Lait Spots, Oligodendroglioma and Rectal CancerSemantic proximity Read ↗

An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation.Semantic proximity Read ↗

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