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Saudi Journal of Kidney Diseases and Transplantation
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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

Year : 2012| Volume: 23| Issue : 5 | Page no: 1038-1042

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