Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation

In a large cohort of osteogenesis imperfecta type V (OI type V) patients (17 individuals from 12 families), we identified the same mutation in the 5′ untranslated region (5′UTR) of the interferon-induced transmembrane protein 5 (IFITM5) gene by whole exome and Sanger sequencing (IFITM5 c.–14C > T...

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Detalles Bibliográficos
Autores principales: Shapiro, Jay R, Lietman, Caressa, Grover, Monica, Lu, James T, Nagamani, Sandesh CS, Dawson, Brian C, Baldridge, Dustin M, Bainbridge, Matthew N, Cohn, Dan H, Blazo, Maria, Roberts, Timothy T, Brennen, Feng-Shu, Wu, Yimei, Gibbs, Richard A, Melvin, Pamela, Campeau, Philippe M, Lee, Brendan H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688672/
https://www.ncbi.nlm.nih.gov/pubmed/23408678
http://dx.doi.org/10.1002/jbmr.1891

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688672/
https://www.ncbi.nlm.nih.gov/pubmed/23408678
http://dx.doi.org/10.1002/jbmr.1891

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