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

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 disab...

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Detalles Bibliográficos
Autores principales: Lindholm Carlström, Eva, Halvardson, Jonatan, Etemadikhah, Mitra, Wetterberg, Lennart, Gustavson, Karl-Henrik, Feuk, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833288/
https://www.ncbi.nlm.nih.gov/pubmed/31694657
http://dx.doi.org/10.1186/s12920-019-0606-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833288/
https://www.ncbi.nlm.nih.gov/pubmed/31694657
http://dx.doi.org/10.1186/s12920-019-0606-4

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