For citations:

Grebennikova T.A., Gavrilova A.O., Tiulpakov A.N., Tarbaeva N.V., Belaya Zh.E., Melnichenko G.A. First description of a type v osteogenesis imperfecta clinical case with severe skeletal deformities caused by a mutation p.119C> T in IFITM5 gene in Russia. Osteoporosis and Bone Diseases. 2019;22(2):32-37. (In Russ.)