Circadian Abnormalities in Mouse Models of Smith–Magenis Syndrome: Evidence for Involvement of RAI1
Smith–Magenis syndrome (SMS; OMIM 182290) is a genomic disorder characterized by multiple congenital anomalies, intellectual disability, behavioral abnormalities, and disordered sleep resulting froman ~3.7 Mb deletion copy number variant (CNV) on chromosome 17p11.2 or from point mutations in the gen...
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| Hoofdauteurs: | , , |
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| Formaat: | Text |
| Taal: | Engels |
| Gepubliceerd in: |
2013
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| Onderwerpen: | |
| Online toegang: | https://pmc.ncbi.nlm.nih.gov/articles/PMC4086898/ https://pubmed.ncbi.nlm.nih.gov/23703963 http://dx.doi.org/10.1002/ajmg.a.35941 |
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