Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder

Smith-Magenis syndrome (SMS), linked to Retinoic Acid Induced (RAI1) haploinsufficiency, is a unique model of the inversion of circadian melatonin secretion. In this regard, this model is a formidable approach to better understand circadian melatonin secretion cycle disorders and the role of the RAI...

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Detalles Bibliográficos
Autores principales: Poisson, Alice, Nicolas, Alain, Bousquet, Idriss, Raverot, Véronique, Gronfier, Claude, Demily, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679101/
https://www.ncbi.nlm.nih.gov/pubmed/31330985
http://dx.doi.org/10.3390/ijms20143533

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679101/
https://www.ncbi.nlm.nih.gov/pubmed/31330985
http://dx.doi.org/10.3390/ijms20143533

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