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This syndrome is caused by a germline mutation in the MEN1 tumor suppressor gene and has a prevalence of 23 per 100,000 [34,35]

Predominantly located in the ganglion cell layer of the retina with additional sparse expression detected in the inner nuclear layer and outer nuclear layer, GLP-1R was found to be expressed at high levels in the retina, even surpassing in tissues like the liver and bowel

[DOI] [PubMed] [Google Scholar] 858.Mieczkowska A., Irwin N., Flatt P.R., Chappard D., Mabilleau G

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