2011年

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上一条:3. Chiang PW, Wang J, Chen Y, Fu Q, Zhong J, Chen Y, Yi X, Wu R, Gan H, Shi Y, Chen Y, Barnett C, Wheaton D, Day M, Sutherland J, Heon E, Weleber RG, Gabriel LA, Cong P, Chuang K, Ye S, Sallum JM, Qi M (2012). Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis. Nat Genet. 44:972-4 下一条:1. Shi N, Zeng W, Ye S, Li Y, Jiang Y (2011). Crucial Points within the Pore as Determinants of K(+) Channel Conductance and Gating. J Mol Biol, 411:27-35