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A recurrent mutation in the 5′-UTR of IFITM5 causes osteogenesis imperfecta type V


  • Conflict of interest: none.

Correspondence to:

Dr. Tomonobu Hasegawa, M.D., Ph.D., Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan. E-mail:

No abstract is available for this article.