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Structural study of a mutant type I collagen from a patient with osteogenesis imperfecta

✍ Scribed by Traub, W.; Steinmann, B.

Book ID
122971511
Publisher
Elsevier Science
Year
1986
Tongue
English
Weight
150 KB
Volume
7
Category
Article
ISSN
8756-3282

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## Communicated by Richard G.H. Cotton Mutations in the type I collagen genes COL1A1 and COL1A2 are responsible for the dominantly inherited connective tissue disorder osteogenesis imperfecta (OI). The severity of OI is diverse, ranging from perinatal lethality to a very mild phenotype that is cha