Author:
Brenner E. V.,Smagulova F. O.,Morozov I. V.
Reference10 articles.
1. Zschocke, J., Phenylketonuria Mutations in Europe, Hum. Mutat., 2003, vol. 21, no. 4, pp. 345–356.
2. Byck, S., Morgan, K., Tyfield, L., et al., Evidence for Origin, by Recurrent Mutation, of the Phenylalanine Hydroxylase R408W Mutation on Two Haplotypes in European and Quebec Populations, Hum. Mol. Genet., 1994, vol. 3, no. 9, pp. 1675–1677.
3. Zschocke, J. and Hoffmann, G., Phenylketonuria Mutations in Germany, Hum. Genet., 1999, vol. 104, no. 5, pp. 390–398.
4. Mallolas, J., Vilaseca, M.A., Campistol, J., et al., Clinical, Biomedical, Neurological and Molecular Study of 11 Patients with New Mutations in PAH Gene, Rev. Neurol., 2000, vol. 31, no. 10, pp. 907–910.
5. Smagulova, F.O., Brenner, E.V., Kotova, L.Yu., et al., Identification of Mutation of the Phenylalanine Hydroxylase Gene Using an Automated Genetic Analyzer, Russ. J. Genet., 2004, vol. 40, no. 2, pp. 208–211.