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Saudi Journal of Kidney Diseases and Transplantation
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Year : 2012 | Volume:  23 | Issue Number:  5

CASE REPORT

Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRMP6 gene mutation

Habeb Abdelhadi M, Al-Harbi Hanan, Schlingmann Karl P

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