An analysis of osteoporosis in patients with hereditary multiple exostoses

被引:0
作者
K. Matsumoto
H. Ogawa
S. Nozawa
H. Akiyama
机构
[1] Gifu University,Department of Orthopaedic Surgery
[2] Graduate School of Medicine,undefined
来源
Osteoporosis International | 2020年 / 31卷
关键词
Heparan sulfate; Hereditary multiple exostoses; Osteoporosis;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:2355 / 2361
页数:6
相关论文
共 205 条
  • [1] Akita S(2007)Long-term results of surgery for forearm deformities in patients with multiple cartilaginous exostoses J Bone Joint Surg Am 89 1993-1999
  • [2] Murase T(2015)Scoliosis in patients with multiple hereditary exostoses Eur Spine J 24 1568-1573
  • [3] Yonenobu K(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 10932-10937
  • [4] Shimada K(1995)Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1) Nat Genet 11 137-143
  • [5] Masada K(1996)The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes Nat Genet 14 25-32
  • [6] Yoshikawa H(1997)Genomic organization and promoter structure of the human EXT1 gene Genomics. 40 351-354
  • [7] Matsumoto Y(1997)The structure of the human multiple exostoses 2 gene and characterization of homologs in mouse and Caenorhabditis elegans Genome Res 7 359-367
  • [8] Matsumoto K(2013)Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas Sci Rep 3 1346-188
  • [9] Harimaya K(2014)Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses J Appl Genet 55 183-62
  • [10] Okada S(2001)Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses Am J Med Genet 99 59-50