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PMID: 27081514 Published · epublish English

Osteogenesis imperfecta IIC caused by a novel heterozygous mutation in the C-propeptide region of COL1A1.

Human genome variation ·Vol. 1 ·2016-04-15

Takagi Masaki, Matsushita Mitsuru, Nishimura Gen, Hasegawa Tomonobu

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.

Article Info
Journal
Human genome variation
Abbr.
Hum Genome Var
ISSN
2054-345X
Published
2016-04-15
Indexed
2016-04-15
Updated
2016-04-18
Language
English
Country/Region
England
NLM ID
101652445
External Links
PubMed source
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