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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Publicado no:Neuron
Main Authors: Huang, Wei-Hsiang, Guenthner, Casey J., Xu, Jin, Nguyen, Tiffany, Schwarz, Lindsay A., Wilkinson, Alex W., Gozani, Or, Chang, Howard Y., Shamloo, Mehrdad, Luo, Liqun
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha: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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