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J Mol Med (2005) 83:33–38
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The online version of the original article can be found at http://dx.doi.org/10.1007/s00109-004-0610-8
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Frishberg, Y., Topaz, O., Bergman, R. et al. Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders. J Mol Med 83, 240 (2005). https://doi.org/10.1007/s00109-005-0654-4
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DOI: https://doi.org/10.1007/s00109-005-0654-4