Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2mutations in isolated AMRF features

AMRF is a genetic neurological disease involving mutations to the SCARB2 gene. SCARB2 is also the main enterovirus 71 receptor (also 3 other EV types). Not only are the symptoms similar, they also improve with alcohol, like some of my symptoms... https://