E. Pras
Department of Medicine C
Chaim Sheba Medical Center
Tel-Hashomer
Israel
Name/email consistency: high
- A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family. Pras, E., Frydman, M., Levy-Nissenbaum, E., Bakhan, T., Raz, J., Assia, E.I., Goldman, B., Pras, E. Invest. Ophthalmol. Vis. Sci. (2000)
- Cystinuria at the turn of the millennium: clinical aspects and new molecular developments. Pras, E. Mol. Urol (2000)
- Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1 using historical recombinants in Libyan Jewish cystinuria patients. Pras, E., Kreiss, Y., Frishberg, Y., Prosen, L., Aksentijevich, I., Kastner, D.L. Genomics (1999)
- Biochemical and clinical studies in Libyan Jewish cystinuria patients and their relatives. Pras, E., Kochba, I., Lubetzky, A., Pras, M., Sidi, Y., Kastner, D.L. Am. J. Med. Genet. (1998)
