Author:
Singh Virender,Rai Ratan Kumar,Arora Ashish,Sinha Neeraj,Thakur Ashwani Kumar
Publisher
Springer Science and Business Media LLC
Reference50 articles.
1. Blau, N., van Spronsen, F. J. & Levy, H. L. Phenylketonuria. Lancet 376, 1417–1427 (2010).
2. Williams, R. A., Mamotte, C. D. & Burnett, J. R. Phenylalanine: an inborn error of phenylalanine metabolism. Clin. Biochem. Rev. 29, 31–41 (2008).
3. Mitchell, J. J., Trakadis, Y. J. & Scriver, C. R. Phenylalanine hydroxylase deficiency. Genet. Med. 13, 697–707 (2011).
4. Kaufman, S. A model of human phenylalanine metabolism in normal subjects and in phenylketonuric patients. Proc. Natl. Acad. Sci. U. S. A. 96, 3160–3164 (1999).
5. Adler-Abramovich, L. et al. Phenylalanine assembly into toxic fibrils suggests amyloid etiology in phenylketonuria. Nat. Chem. Biol. 8, 701–706 (2012).
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