Funder
the scientific and technological research council of turkey
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Applied Microbiology and Biotechnology,Biochemistry,General Medicine,Bioengineering,Biotechnology
Reference34 articles.
1. Blau, N., Van Spronsen, F. J., & Levy, H. L. (2010). Phenylketonuria. The Lancet, 376(9750), 1417–1427.
2. Ikeda, K., Schiltz, E., Fujii, T., Takahashi, M., Mitsui, K., Kodera, Y., & Nishimura, H. (2005). Phenylalanine ammonia-lyase modified with polyethylene glycol: Potential therapeutic agent for phenylketonuria. Amino Acids, 29(3), 283–287.
3. Levy, H. L., Sarkissian, C. N., & Scriver, C. R. (2018). Phenylalanine ammonia lyase (PAL): From discovery to enzyme substitution therapy for phenylketonuria. Molecular Genetics and Metabolism, 124(4), 223–229.
4. Sumaily, K. M., & Mujamammi, A. H. (2017). Phenylketonuria: A new look at an old topic, advances in laboratory diagnosis, and therapeutic strategies. International Journal of Health Sciences, 11(5), 63.4.
5. Vardy, E. R., MacDonald, A., Ford, S., & Hofman, D. L. (2020). Phenylketonuria, co-morbidity, and ageing: A review. Journal of Inherited Metabolic Disease, 43(2), 167–178.
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献