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Article

Further evidence for distinct traits associated with RBM10 missense variants.

Clinical genetics - 1 Aug 2022

Poulton Cathryn, Baynam Gareth, Pugh Kye, Mason Michael, Kiraly-Borri Catherine, Gration Dylan, Dreyer Lauren, Viti Leon, Agostino Mark, Heng Julian Ik-Tsen

Abstract excerpt

A case of a missense RBM10 variant in an adult with mild to moderate intellectual disability.

Read the complete abstract on PubMed

Topics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 35645043
DOI: 10.1111/cge.14163

Genes

RBM10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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