A structural mutation of the collagen alpha 1(I)CB7 peptide in lethal perinatal osteogenesis imperfecta.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference33 articles.
1. Genetic heterogeneity in osteogenesis imperfecta.
2. The Proteins;Bornstein,1979
3. Heritable Diseases of Collagen
4. Collagen genes and inherited connective tissue disease
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1. Bilateral congenital cataracts result from a gain-of-function mutation in the gene for aquaporin-0 in mice;Genomics;2003-04
2. 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;Matrix Biology;1998-12
3. The Nicholas Andry Award-1996 The Molecular Pathology of Osteogenesis Imperfecta;Clinical Orthopaedics and Related Research;1997-10
4. Deposition and selective degradation of structually-abnormal type I collagen in a collagen matrix produced by osteogenesis imperfecta fibroblasts in vitro;Matrix Biology;1994-04
5. Chemical cleavage method for the detection of RNA base changes: Experience in the application to collagen mutations in osteogenesis imperfecta;American Journal of Medical Genetics;1993-01-15
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