Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosis

Author:

Steiner R. D.1,Whyte M. P.2,Chang E.3,Hanks J.3,Mattes C.4,Senephansiri H.4,Gibson K. M.4

Affiliation:

1. ; Departments of Pediatrics and Molecular and Medical Genetics; Oregon Health Sciences University; Portland Oregon USA

2. ; Metabolic Research Unit, Shriners Hospital for Children and Division of Bone and Mineral Diseases; Washington University School of Medicine; St Louis Missouri USA

3. ; Department of Pediatrics; St Luke's Regional Medical Center; Boise Idaho USA

4. ; Department of Molecular and Medical Genetics; Oregon Health Sciences University; Portland Oregon USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference7 articles.

1. Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation;Heaney;Hum Mol Genet,1998

2. Abnormal urinary excretion of glycosaminoglycans in Albers-Schonberg disease;Marcucci;Clin Chim Acta,1982

3. The putative tumour suppressor EXT1 alters the expression of cell-surface heparan sulfate;McCormick;Nature Genetics,1998

4. Structure, chromosomal location, and expression profile of EXTR1 and EXTR2, new members of the multiple exostoses gene family;Saito;Biochem Biophys Res Commun,1998

5. Increased urine heparan and chondroitin sulfate excretion in a patient with malignant osteopetrosis (OP): clues to pathogenesis?;Steiner;Am J Hum Genet,1998

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