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  1. 1
    Nobutaka Hanagata, IFITM5 mutations and osteogenesis imperfecta, Journal of Bone and Mineral Metabolism, 2015,

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  2. 2
    Heike Hoyer-Kuhn, Oliver Semler, Lutz Garbes, Katharina Zimmermann, Jutta Becker, Bernd Wollnik, Eckhard Schoenau, Christian Netzer, A Nonclassical IFITM5 Mutation Located in the Coding Region Causes Severe Osteogenesis Imperfecta With Prenatal Onset, Journal of Bone and Mineral Research, 2014, 29, 6
  3. 3
    Syndia Lazarus, Aideen M McInerney-Leo, Fiona A McKenzie, Gareth Baynam, Stephanie Broley, Barbra V Cavan, Craig F Munns, Johannes Egbertus Pruijs, David Sillence, Paulien A Terhal, Karena Pryce, Matthew A Brown, Andreas Zankl, Gethin Thomas, Emma L Duncan, The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V, BMC Musculoskeletal Disorders, 2014, 15, 1, 107

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    Encarna Guillén-Navarro, María Juliana Ballesta-Martínez, María Valencia, Ana María Bueno, Victor Martinez-Glez, Vanesa López-González, Birute Burnyte, Algirdas Utkus, Pablo Lapunzina, Victor L. Ruiz-Perez, Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta, American Journal of Medical Genetics Part A, 2014, 164, 5
  5. 5
    Jill M. Perreira, Christopher R. Chin, Eric M. Feeley, Abraham L. Brass, IFITMs Restrict the Replication of Multiple Pathogenic Viruses, Journal of Molecular Biology, 2013, 425, 24, 4937

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