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

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

Smith-Magenis syndrome (SMS), linked to <i>Retinoic Acid Induced</i> (<i>RAI1</i>) 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 c...

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Bibliographic Details
Main Authors: Alice Poisson, Alain Nicolas, Idriss Bousquet, Véronique Raverot, Claude Gronfier, Caroline Demily
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:International Journal of Molecular Sciences
Subjects:
circadian clock
circadian cycle
melatonin
neurogenetics
<i>RAI1</i>
<i>CLOCK</i>
Online Access:https://www.mdpi.com/1422-0067/20/14/3533

Internet

https://www.mdpi.com/1422-0067/20/14/3533

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