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Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability
Families with multiple male children with intellectual disability (ID) are usually suspected of having disease due to a X-linked mode of inheritance and genetic studies focus on analysis of segregating variants in X-linked genes. However, the genetic cause of ID remains elusive in approximately 50%...
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| Publicat a: | Front Genet |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6609311/ https://ncbi.nlm.nih.gov/pubmed/31316545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00578 |
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