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 - Concepedia

Concepedia

Publication | Open Access

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

DOI Full Paper Access

21

Citations

23

References

2014

Year

Syndia Lazarus, Aideen McInerney‐Leo, Fiona A. McKenzie, Gareth Baynam, Stephanie Broley, Barbra V Cavan, Craig F. Munns, J. E. H. Pruijs, David Sillence, Karena Pryce,

BMC Musculoskeletal Disorders

References

	Year	Citations

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