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A Case Report of Familial Benign Hypocalciuric Hypercalcemia: A Mutation in the Calcium-Sensing Receptor Gene

Woo SI, Song H, Song KE, Kim DJ, Lee KW, Kim SJ, Chung YS

Familial benign hypocalciuric hypercalcemia (FBHH) is an autosomal dominant trait with high penetrance, clinically manifestating a relatively benign, lifelong, persistent hypercalcemia and hypocalciuria without hypercalcemic related complications. The calcium-sensing receptor...
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Inherited canine copper toxicosis in Australian Bedlington Terriers

Hyun C, Filippich

  • KMID: 1094684
  • J Vet Sci.
  • 2004 Mar;5(1):19-28.
Inherited copper toxicosis in Bedlington Terriers (CTBT) is a copper associated hepatopathy caused by an autosomal recessive genetic defect of gene involving copper metabolism. To compare clinical and histopathological findings...
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