Absence ofFKBP10in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix-Reference-Cited by-同舟云学术

Absence ofFKBP10in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix

Published:2012-07-16 Issue:11 Volume:33 Page:1589-1598
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Barnes Aileen M.,Cabral Wayne A.,Weis MaryAnn,Makareeva Elena,Mertz Edward L.,Leikin Sergey,Eyre David,Trujillo Carlos,Marini Joan C.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference42 articles.

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3. Biochemical changes in the collagen of human osteoporotic bone matrix;Bailey;Connect Tissue Res,1993

4. Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding;Barnes;N Engl J Med,2010

5. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta;Barnes;N Engl J Med,2006

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