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Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C
Keun Hee Choi (Choi KH), Choong Ho Shin (Shin CH), Sei Won Yang (Yang SW), Hae Il Cheong (Cheong HI)
Clin Exp Pediatr. 2015;58(4):148-153. Published online 2015 Apr 22 DOI: https://doi.org/10.3345/kjp.2015.58.4.148
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