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Rafaelsen S, Johansson S, R\u00e6der H, Bjerknes R. Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature. BMC Genet. 2014; 15:98.","DOI":"10.1186\/s12863-014-0098-3"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Sun L, Zhao L, Du L, Zhang P, Zhang M, Li M, Liu T, Ye L, Tao B, Zhao H, Liu J, Ding X. Identification of two novel mutations in the <i>GALNT3<\/i> gene in a Chinese family with hyperphosphatemic familial tumoral calcinosis. Bone Res. 2016; 4:16038.","DOI":"10.1038\/boneres.2016.38"},{"key":"6","doi-asserted-by":"crossref","unstructured":"7. Joseph L, Hing SN, Presneau N, O&apos;Donnell P, Diss T, Idowu BD, Joseph S, Flanagan AM, Delaney D. Familial tumoral calcinosis and hyperostosis-hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3. 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