Serum prolactin as a tool for the follow-up of treated DHPR-deficient patients
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-007-0788-3
Reference15 articles.
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3. Danks DM, Schlesinger P, Firgaira F et al (1979) Malignant hyperphenylalaninemia—clinical features, biochemical findings, and experience with administration of biopterins. Pediatr Res 13: 1150–1155.
4. de Sanctis L, Alliaudi C, Spada M et al (2000) Genotype–phenotype correlation in dihydropteridine reductase deficiency. J Inherit Metab Dis 23: 333–337.
5. Dianzani I, Howells DW, Ponzone A, Saleeba JA, Smooker PM, Cotton RGH (1993) Two new mutations in the dihydropteridine reductase gene in patients with tetrahydrobiopterin deficiency. J Med Genet 30: 465–469.
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