Abstract
We read with great interest the recent report by Morice-Picard et al. (2020) on how mutations in SREBF1 (Online Mendelian Inheritance in Man: 184756) are associated with hereditary mucoepithelial dysplasia (HMD) (Online Mendelian Inheritance in Man: 158310). SREBF1 encodes SREBP1, which is involved in promoting the transcription of lipogenes that are associated with cholesterol and fatty acid biosynthesis (Zhang et al., 2017).
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