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A mutation in the amino-terminal end of the triple helix of type II collagen causing severe osteochondrodysplasia.

Bibliographic reference Vikkula, Miikka ; Ritvaniemi, P ; Vuorio, A F ; Kaitila, I ; Ala-Kokko, L ; et. al. A mutation in the amino-terminal end of the triple helix of type II collagen causing severe osteochondrodysplasia.. In: Genomics, Vol. 16, no.1, p. 282-5 (1993)
Permanent URL http://hdl.handle.net/2078.1/120823