From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes
暂无分享,去创建一个
R. Salomon | J. Rendu | B. Ranchin | N. Monnier | J. Lunardi | C. Coutton | A. Blanchard | V. Satre | Haifa Hichri | O. Dorseuil | R. Poussou | G. Baujat | F. Nobili | M. Remesy