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Abnormally low lysine in insoluble dentine from patients with osteogenesis imperfecta

✍ Scribed by Francis, M.J.O.; Gage, J.P.; Smith, R.

Book ID
122718058
Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
137 KB
Volume
6
Category
Article
ISSN
8756-3282

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Various mutations of genes encoding type I procollagen chains have been linked to osteogenesis imperfecta (OI). The mutations yield abnormal procollagen molecules that fold improperly. HSP 47, a stress-inducible protein localized to the endoplasmic reticulum (ER) of collagen-producing cells, may par