Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism.
paper
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- Authors
- Bhat, S S; Ladd, S; Grass, F; Spence, J E; Brasington, C K; Simensen, R J; Schwartz, C E; Dupont, B R; Stevenson, R E; Srivastava, A K
- Year
- 2008
- Journal
- Clinical genetics
- PMID
- 18005360
- DOI
- 10.1111/j.1399-0004.2007.00920.x
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In this knowledge base
| Title | Year | PMID |
|---|---|---|
| Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. | 2010 | 20844286 |
External
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| Loss of SETDB1 decompacts the inactive X chromosome in part through reactivation of an enhancer in the IL1RAPL1 gene. | Sun Z et al. | β | 2018 | β |
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