Analysis of phenylalanine hydroxylase gene mutations in phenylketonuria patients from Kemerovo oblast and the Sakha Republic-Reference-Cited by-同舟云学术

Analysis of phenylalanine hydroxylase gene mutations in phenylketonuria patients from Kemerovo oblast and the Sakha Republic

Published:2012-07 Issue:4 Volume:46 Page:227-232
ISSN:0095-4527
Container-title:Cytology and Genetics
language:en
Short-container-title:Cytol. Genet.

Author:

Baturina O. A.,Bondar A. A.,Tupikin A. E.,Zhabin S. G.,Morozov I. V.

Publisher

Allerton Press

Subject

Genetics,Agricultural and Biological Sciences (miscellaneous),Cell Biology

Link

http://link.springer.com/content/pdf/10.3103/S0095452712040032.pdf

Reference38 articles.

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2. Lebedev, B.V. and Blyumina, M.V., Fenilketonuriya u detei (Phenylketonuria in Children), Moscow: Meditsina, 1972.

3. Knivsberg, A.M., Reichelt, K.L., Hoien, T., and Nodland, M., A Randomized, Controlled Study of Dietary Intervention in Autistin Syndromes, Nutr. Meurosci, 2002, vol. 5, no. 5, pp. 251–261.

4. Borinsenko, T.N., Burova, Yu.S., and Khisamova, Kh.A., Children with Phenylketonuria: Features of Psychoverbal Development and the Prospects of a Comprehensive Rehabilitation, Logoped, 2007, no. 1.

5. Neil, C.A., Eisensmith, R.C., Croke, D.T., et al., Molecular Analysis of PKU in Ireland, Acta Paediatr., 1994, vol. 407(Suppl.), pp. 43–46.

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