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

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

Abstract 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 intellectu...

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Bibliographic Details
Main Authors: Eva Lindholm Carlström, Jonatan Halvardson, Mitra Etemadikhah, Lennart Wetterberg, Karl-Henrik Gustavson, Lars Feuk
Format: Article
Language:English
Published: BMC 2019-11-01
Series:BMC Medical Genomics
Subjects:
Affymetrix genome-wide human SNP Array 6.0
Complex disorder
Genome wide analysis
Large pedigree
Sequencing
Online Access:http://link.springer.com/article/10.1186/s12920-019-0606-4

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http://link.springer.com/article/10.1186/s12920-019-0606-4

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