Sporadic hyperphosphatasia syndrome featuring periostitis and accelerated skeletal turnover without receptor activator of nuclear factor-κB, osteoprotegerin, or sequestosome-1 gene defects

Suat Simsek, Natalja M. Basoski, Nathalie Bravenboer, Xiafang Zhang, Steven Mumm, Michael P. Whyte, J. Coen Netelenbos

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