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Original Article

The role of carbonic anhydrase in autosomal dominant osteopetrosis

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Pages 93-95 | Received 21 Jan 1988, Accepted 27 Jul 1988, Published online: 08 Jul 2009

References

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  • Marks S C, Jr. Osteopetrosis in the toothless (tl) rat: Presence of osteoclasts but failure to respond to parathyroid extract or to be cured by infusion of spleen or bone marrow cells from normal littermates. Am J Anat 1977; 149: 289–97
  • Marks S C, Jr. Morphological evidence of reduced bone resorption in osteopetrotic (op) mice. Am J Anat 1982; 163: 157–67
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  • Sly W S, Hawett-Emmett D, Whyte M P, Yu Y-S L, Tashian R E. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. Proc Natl Acad Sci, USA 1983; 80: 2725–6
  • Bollerslev J. Osteopetrosis. A genetic and epidemiological study. Clin Gen 1987; 31: 86–90
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  • Baron R, Vigney A, Horowitz M. Lymphocytes, Macrophages and the regulation of bone remodeling. Bone and Mineral Research, Ann 2, W A Peck. Elsevier Science Publishers, Amsterdam 1983; 175–243

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