Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation

P.A. Bell, K.A. Pirõg, M. Fresquet, D.J. Thornton, R.P. Boot-Handford, M.D. Briggs

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Biochemistry, Genetics and Molecular Biology