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A case of familial tumoral calcinosis/hyperostosis–hyperphosphatemia syndrome due to a compound heterozygous mutation inGALNT3demonstrating new phenotypic features

✍ Scribed by C. E. Dumitrescu; M. H. Kelly; A. Khosravi; T. C. Hart; J. Brahim; K. E. White; E. G. Farrow; M. H. Nathan; M. D. Murphey; M. T. Collins

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