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Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)

BACKGROUND: Infantile cortical hyperostosis (ICH)/Caffey disease is an inflammatory collagenopathy of infancy, manifested by subperiosteal bone hyperplasia. Genetically, ICH was linked with heterozygosity for an R836C mutation in the COL1A1 gene. Although an autosomal-recessive trait is also suspect...

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Detalles Bibliográficos
Autores principales:	Merdler-Rabinowicz, Rona, Grinberg, Anna, Jacobson, Jeffrey M., Somekh, Ido, Klein, Christoph, Lev, Atar, Ihsan, Salama, Habib, Adib, Somech, Raz, Simon, Amos J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group US 2019
Materias:	Basic Science Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086575/ https://www.ncbi.nlm.nih.gov/pubmed/31288248 http://dx.doi.org/10.1038/s41390-019-0499-0

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