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doi: 10.1093/plphys/kiab600 22 LiN.ShangJ

Myelin breakdown and iron changes in Huntington's disease: pathogenesis and treatment implications
Intestinal dysbiosis and hormonal neuroendocrine secretion in the fibromyalgic patient
These include 1) congenital pernicious anaemia, where there is a genetic defect in IF synthesis, leading to B12 malabsorption, 2) Imerslund-Grsbeck Syndrome (IGS) caused by mutations in genes encoding cubulin and amnionless , 3) inherited HC or TCII deficiencies, and 4) intracellular cobalamin defects (CblA-CblG defects)