Alterations of bone material properties in growing Ifitm5/BRIL p.S42 knock-in mice, a new model for atypical type VI osteogenesis imperfecta-Reference-Cited by-同舟云学术

Alterations of bone material properties in growing Ifitm5/BRIL p.S42 knock-in mice, a new model for atypical type VI osteogenesis imperfecta

Published:2022-09 Issue: Volume:162 Page:116451
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Hedjazi Ghazal,Guterman-Ram Gali,Blouin Stéphane,Schemenz Victoria,Wagermaier Wolfgang,Fratzl Peter,Hartmann Markus A.,Zwerina Jochen,Fratzl-Zelman Nadja,Marini Joan C.

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference88 articles.

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4. Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen;Willing;Am. J. Hum. Genet.,1992

5. Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue;Prockop;Am. J. Med. Genet.,1989

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