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Fleury, V.P., Hedges, S., Hume, K., Browder, D.M., Thompson, J.L., Fallin, K., El Zein, F., Reutebuch, C.K., and Vaughn, S., Remedial and Special Education , 2014, vol

CHS molecule can be docked in two planar densities on the opposite side of the PIP 2 -channel interface

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Wilson disease (WD) is an autosomal recessive disorder caused by mutations in ATP7B that is primarily due to ATP7B mutations that result in impaired copper excretion from hepatocytes into bile, a significant increase in copper levels in hepatocytes and subsequent liver injury