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

• Päätekijät: Eva Lindholm Carlström (Tekijä), Jonatan Halvardson (Tekijä), Mitra Etemadikhah (Tekijä), Lennart Wetterberg (Tekijä), Karl-Henrik Gustavson (Tekijä), Lars Feuk (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: BMC, 2019-11-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

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...