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Nicholls A.C., Oliver J., McCarron S., Winter G.B., Pope F.M. Splice site mutation causing deletion of exon 21 sequences from the pro-alpha-2(I) chain of type I collagen in a patient with severe dentinogenesis imperfecta but very mild osteogenesis imperfecta. - Hum.Mut., 1996, v. 7, p. 219-227.

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