Found: 2

Select item for more details and to access through your institution.

  • SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 5, p. 656, doi. 10.1093/hmg/ddm337
    By:
    • Vithana, Eranga N.;
    • Morgan, Patricio E.;
    • Ramprasad, Vedam;
    • Tan, Donald T.H.;
    • Yong, Victor H.K;
    • Venkataraman, Divya;
    • Venkatraman, Anandalakshmi;
    • Yam, Gary H.F.;
    • Nagasamy, Soumittra;
    • Law, Ricky W.K.;
    • Rajagopal, Rama;
    • Pang, Chi P.;
    • Kumaramanickevel, Govindsamy;
    • Casey, Joseph R.;
    • Aung, Tin
    Publication type:
    Article

  • Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2).

    Published in:
    Human Mutation, 2007, v. 28, n. 5, p. 522, doi. 10.1002/humu.9487
    By:
    • Ramprasad, Vedam L.;
    • Ebenezer, Neil D.;
    • Aung, Tin;
    • Rajagopal, Rama;
    • Yong, Victor H.K.;
    • Tuft, Stephen J.;
    • Viswanathan, Deepa;
    • El-Ashry, Mohamed F.;
    • Liskova, Petra;
    • Tan, Donald T.H.;
    • Bhattacharya, Shomi S.;
    • Kumaramanickavel, Govindasamy;
    • Vithana, Eranga N.
    Publication type:
    Article