Imerslund-Grasbeck Syndrome (IGS) is a rare genetic disorder characterised by juvenile megaloblastic anaemia. IGS is caused by mutations in either of the genes encoding the intestinal intrinsic factor-vitamin B12 receptor complex, cubam.
The cubam receptor proteins cubilin and amnionless are…
Detailed investigations of proximal tubular function in Imerslund-Grasbeck syndrome
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