An analysis of osteoporosis in patients with hereditary multiple exostoses
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s00198-020-05533-7.pdf
Reference30 articles.
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2. Matsumoto Y, Matsumoto K, Harimaya K, Okada S, Doi T, Iwamoto Y (2015) Scoliosis in patients with multiple hereditary exostoses. Eur Spine J 24(7):1568–1573
3. Matsumoto K, Irie F, Mackem S, Yamaguchi Y (2010) A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses. Proc Natl Acad Sci U S A 107(24):10932–10937
4. Ahn J, Ludecke HJ, Lindow S, Horton WA, Lee B, Wagner MJ, Horsthemke B, Wells DE (1995) Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1). Nat Genet 11(2):137–143
5. Stickens D, Clines G, Burbee D, Ramos P, Thomas S, Hogue D, Hecht JT, Lovett M, Evans GA (1996) The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes. Nat Genet 14(1):25–32
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