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Description
The rare autosomal recessive disorder Immerslund-Grasbeck (IGS) disease is caused by mutations in either the gene Amnion Associated Transmembrane Protein (AMN) or Cubilin (CUBN) gene responsible for the synthesis of cubam receptors (Sobczynska-Malefora et al., 2021)
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Subsidence of the ventricular effects may be followed by atrial tachycardia and occasionally by atrioventricular block
