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Article

Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.

BMC medical genomics - 6 Nov 2019

Lindholm Carlström Eva, Halvardson Jonatan, Etemadikhah Mitra, Wetterberg Lennart, Gustavson Karl-Henrik, Feuk Lars

Abstract excerpt

BACKGROUND: Non-syndromic intellectual disability is genetically heterogeneous with dominant, recessive and complex forms of inheritance. We have performed detailed genetic studies in a large multi-generational Swedish family, including several members diagnosed with non-syndromic intellectual disability. Linkage analysis was performed on 22 family members, nine affected with mild to moderate intellectual...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31694657
DOI: 10.1186/s12920-019-0606-4
PMCID: PMC6833288

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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