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Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis
Published on: December 18, 2019
A novel COL1A1 mutation in a family with osteogenesis imperfecta associated with phenotypic variabilities
Toshiyuki Seto1, Toshiyuki Yamamoto2, Keiko Shimojima2
1Department of Pediatrics, Graduate School of Medicine, Osaka City University , Osaka, Japan.
Abstract:
Osteogenesis imperfecta (OI) is a heterogeneous disorder that is characterized by bone fragility and systemic complications, and is mainly caused by gene mutations in COL1A1 or COL1A2. A novel COL1A1 splicing mutation, c.750+2T>A, was identified in a Japanese OI family. Only the proband in this family showed various complications, such as heart valve diseases and severe scoliosis. The clinical heterogeneity in the family is discussed in this study.
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