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Article

Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome

1 Jan 2016

Abstract excerpt

gene may be classified as disease-causing for EDS due to tenascin-X deficiency.

Read the complete abstract on PubMed

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 28344932
DOI: 10.5496/wjmg.v6.i2.17

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

Related research

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Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndromePMID 28344932Read ↗

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Well-defined clinical presentation of Ehlers-Danlos syndrome in patients with tenascin-X deficiency: a report of four cases.Semantic proximity Read ↗

The Ehlers-Danlos syndrome.Semantic proximity Read ↗

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Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndromeSemantic proximity Read ↗

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Hypermobile Ehlers-Danlos syndrome: A review and a critical appraisal of published genetic research to date.Semantic proximity Read ↗

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