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[PUBMED Abstract] Mogensen SS, Harila-Saari A, Mkitie O, et al.: Comparing osteonecrosis clinical phenotype, timing, and risk factors in children and young adults treated for acute lymphoblastic leukemia

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of Paediatrics and Child Health, The Aga Khan Univ., Karachi, Pakistan Autosomal recessive hypophosphatemia arises from homozygous inactivating mutations in dentin matrix protein 1 (DMP1), a gene responsible for encoding a noncollagenous bone matrix protein expressed in osteoblasts and osteocytes

doi: 10.1016/j.tibs.2014.06.005 18 ChenLZhangZHoshinoAZhengHDMorleyMAranyZet al

The conjugates formed are usually excreted in the bile, but can also undergo modification to mercapturic acid