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Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability
Intellectual Disability (ID) is a clinically heterogeneous condition that affects 2–3% of population worldwide. In recent years, exome sequencing has been a successful strategy for studies of genetic causes of ID, providing a growing list of both candidate and validated ID genes. In this study, exom...
Zapisane w:
| Wydane w: | Am J Med Genet B Neuropsychiatr Genet |
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| Główni autorzy: | , , , , , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
John Wiley and Sons Inc.
2017
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5765476/ https://ncbi.nlm.nih.gov/pubmed/28990276 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32574 |
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