| Literature DB >> 27081514 |
Masaki Takagi1, Mitsuru Matsushita2, Gen Nishimura3, Tomonobu Hasegawa4.
Abstract
Osteogenesis imperfecta IIC (OI IIC), which is a rare variant of lethal OI that has been considered to be an autosomal recessive trait, is characterized by twisted, slender long bones with dense metaphyseal margins. Here, we report a typical case of OI IIC caused by a novel heterozygous mutation in the C-propeptide region of COL1A1. OI IIC seems to be caused by a dominant mutation of COL1A1.Entities:
Year: 2014 PMID: 27081514 PMCID: PMC4785516 DOI: 10.1038/hgv.2014.25
Source DB: PubMed Journal: Hum Genome Var ISSN: 2054-345X