Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel trmp6 gene mutation
By: Habib, Abd al-Hadi M.; al-Harbi, Hanan A.; Schlingmann, Karl P.. Saudi Journal of Kidney Diseases and Transplantation. Vol. 23, no. 5 (Oct. 2012), pp.1038-1042, 5 p.
Subjects: Magnesium deficiency