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Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis

✍ Scribed by Franco Antoniazzi; Francesco Bertoldo; Monica Mottes; Maurizia Valli; Stefania Sirpresi; Giorgio Zamboni; Roberta Valentini; Luciano Tatò

Book ID
117165224
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
802 KB
Volume
129
Category
Article
ISSN
1097-6833

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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