Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retina.
暂无分享,去创建一个
L. Salviati | M. A. Desbats | I. Bellezza | R. Montioli | B. Cellini | C. Borri Voltattorni | S. Grottelli | Mara Doimo | Silvia Grottelli