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Article

Whole-exome sequencing for finding de novo mutations in sporadic mental retardation.

Genome biology - 1 Jan 2010

Robinson Peter N

Abstract excerpt

Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21172032
DOI: 10.1186/gb-2010-11-12-144
PMCID: PMC3046476

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21172032-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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