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Epigenetic Regulation of Osteogenesis Imperfecta Severity : miROI Study

of COL1A1 or COL1A2, encoding 1 and 2 of the collagen, regardless of their phenotypic severity (1 to 5 OI type). This observation suggests the existence of a undetermined mechanism that may be

col1a1
bone disease
autosomal dominant
col1a2
genetic disorder
  • 4 views
  • 02 May, 2021
  • 2 locations