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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.
Lazarus S, McInerney-Leo AM, McKenzie FA, Baynam G, Broley S, Cavan BV, Munns CF, Pruijs JE, Sillence D, Terhal PA, Pryce K, Brown MA, Zankl A, Thomas G, Duncan EL. Lazarus S, et al. Among authors: brown ma. BMC Musculoskelet Disord. 2014 Mar 27;15:107. doi: 10.1186/1471-2474-15-107. BMC Musculoskelet Disord. 2014. PMID: 24674092 Free PMC article.
Genetic studies of osteoporosis.
Brown MA, Duncan EL. Brown MA, et al. Expert Rev Mol Med. 1999 Oct 19;1999:1-18. doi: 10.1017/S1462399499000964. Expert Rev Mol Med. 1999. PMID: 14585121
Genetic studies in osteoporosis--the end of the beginning.
Duncan EL, Brown MA. Duncan EL, et al. Among authors: brown ma. Arthritis Res Ther. 2008;10(5):214. doi: 10.1186/ar2479. Epub 2008 Sep 12. Arthritis Res Ther. 2008. PMID: 18828878 Free PMC article. Review.
Genetics and genomics of ankylosing spondylitis.
Thomas GP, Brown MA. Thomas GP, et al. Among authors: brown ma. Immunol Rev. 2010 Jan;233(1):162-80. doi: 10.1111/j.0105-2896.2009.00852.x. Immunol Rev. 2010. PMID: 20192999 Review.
1,544 results