Author:
Alibakhshi Reza,Moradi Keyvan,Mohebbi Zahra,Ghadiri Keyghobad
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology,Biochemistry
Reference22 articles.
1. Bickel H, Bachmann C, Beckers R, Brandt NJ, Clayton BE, Corrado G, Feingold HJ, Giardini O, Hammersen G, Schonberg D (1981) Neonatal mass screening for metabolic disorders. Eur J Pediatr 137:133–139
2. Bonyadi M, Omrani O, Moghanjoghi SM, Shiva S (2010) Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuria. Genet Test Mol Biomarkers 14(2):233–235
3. Georgiou T, Ho G, Vogazianos M, Dionysiou M, Nicolaou A, Chappa G, Nicolaides P, Stylianidou G, Christodoulou J, Drousiotou A (2012) The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening. Clin Biochem 45(7–8):588–592
4. Hamzehloei T, Hosseini SA, Vakili R, Mojarad M (2012) Mutation spectrum of the PAH gene in the PKU patients from Khorasan Razavi province of Iran. Gene 506(1):230–232
5. Hashem N, Bosco P, Chiavetta V, Cali F, Ceratto N, Romano V (1996) Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt. Hum Genet 98(1):3–6
Cited by
21 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