Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X
出版年份 2018 全文链接
标题
Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X
作者
关键词
Bisphosphonates, HSP47, Osteogenesis imperfecta, <em class=EmphasisTypeItalic >SERPINH1</em>
出版物
OSTEOPOROSIS INTERNATIONAL
Volume 29, Issue 6, Pages 1389-1396
出版商
Springer Nature
发表日期
2018-03-09
DOI
10.1007/s00198-018-4448-2
参考文献
相关参考文献
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