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Article

A Novel Biallelic STN1 Mutation Is Associated With Adult-Onset Multisystemic Involvement: Broadening the Mutational Spectrum in Coats Plus Syndrome.

Clinical genetics - 1 Apr 2026

Ozen Filiz, Sayit Diyar, Yegin Zeynep

Abstract excerpt

A novel biallelic missense mutation (c.470A>T) in the STN1 gene is responsible for Coats Plus Syndrome.

Read the complete abstract on PubMed

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Source

Identifiers

PMID: 41387117
DOI: 10.1111/cge.70124

Genes

STN1

Variants

Provenance

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

Related research

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Research trail→

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A Novel Biallelic STN1 Mutation Is Associated With Adult-Onset Multisystemic Involvement: Broadening the Mutational Spectrum in Coats Plus Syndrome.PMID 41387117Read ↗

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