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Molecular and Neural Functions of Rai1, The Causal Gene for Smith-Magenis Syndrome
Haploinsufficiency of Retinoic Acid Induced 1 (RAI1) causes Smith-Magenis syndrome (SMS), which is associated with diverse neurodevelopmental and behavioral symptoms as well as obesity. RAI1 encodes a nuclear protein but little is known about its molecular function or the cell types responsible for...
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| Yayımlandı: | Neuron |
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| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5098476/ https://ncbi.nlm.nih.gov/pubmed/27693255 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2016.09.019 |
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