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Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X
Y. Song, D. Zhao, X. Xu, F. Lv, L. Li, Y. Jiang, O. Wang, W. Xia, X. Xing, M. Li*
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
12
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(Scopus)