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doi: 10.1016/j.jhepr.2022.100661

Methods Study design This retrospective, observational cohort study used data from Komodos Healthcare Map to compare outcomes between people using both newer generation GLP-1RA and SGLT2i and those using SGLT2i without GLP-1RA (See Supplementary Fig

Fragile X syndrome is caused by mutations in FMR1 gene (which encodes fragile X mental retardation protein, FMRP) expressed in both neurones and astrocytes

That's all on an intent to attract capital to say when and if we raise this capital, we will allocate it to projects that are credibly green with credible possibilities of outcome and a good governance structure and reporting to do so