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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...
Tallennettuna:
| Julkaisussa: | BMC Med Genomics |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6833288/ https://ncbi.nlm.nih.gov/pubmed/31694657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-019-0606-4 |
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