Pras E.,2000

Pras E., Frydman M., Levy-Nissenbaum E., Bakhan T., Raz J., Assia E.I., Goldman B., Pras E. A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family. - Invest.Ophthal.Iis.Sci., 2000, v. 41, p. 3511-3515.

Ссылки: