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[Citation13] using an alternating oral and IV unithiol (days 116 and 2329) and oral succimer (days 1722 and 3370) reported more mercury (as thiomersal) was excreted in the first 3 days than the entire remaining 70 days of chelation [Citation13]

On the other hand, thorough research using WES revealed that variants that are not presently recognized as pathogenic are significantly frequent in adult patients with cholestatic symptoms, and carriers of these variants should be monitored for various liver pathologies, including tumours [71, 76, 77]

In this case, alternative tags for the targeting of ER-localized zDHHCs to the PM, Golgi or mitochondria might be developed

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