An α2(I) glycine to aspartate substitution is responsible for the presence of a kink in type I collagen in a lethal case of osteogenesis imperfecta

Author:

Forlino Antonella,Keene Douglas R.,Schmidt Karen,Marini Joan C.

Publisher

Elsevier BV

Subject

Molecular Biology

Reference20 articles.

1. Assessment of procollagen processing defects by fibroblasts cultured in the presence of dextran sulphate;Bateman;Biochem. J.,1990

2. A structural mutation of the collagen α1(I)CB7 peptide in lethal perinatal osteogenesis imperfecta;Bateman;J. Biol. Chem.,1987

3. Altered triple helical structure of type I procollagen in lethal perinatal osteogenesis imperfecta;Bonadio;J. Biol. Chem.,1985

4. Osteogenesis Imperfecta;Byers,1993

5. Single step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction;Chomezynsky;Anal. Biochem.,1987

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