Maternal and fetal tyrosinemia type I
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-012-9569-8
Reference10 articles.
1. Cerone R, Fantasia AR, Castellano E, Moresco L, Schiaffino MC, Gatti R (2002) Pregnancy and tyrosinemia type II, case report. J Inherit Metab Dis 25:317–318
2. Chakrapani A, Gissen P, McKiernan P (2012) Disorder of tyrosine metabolism. In: Saudubray JM, Van den Berghe G, Walter JH (eds) Inborn metabolic diseases, diagnosis and treatment, 5th edn. Springer, Heidelberg, pp 265–276
3. Francis DE, Kirby DM, Thompson GN (1992) Maternal tyrosinemia type II: management and successful outcome. Eur J Pediatr 151:196–199
4. Holme E, Lindstedt S (1998) Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione). J Inherit Metab Dis 21:507–517
5. Hostetter MK, Levy HL, Winter HS, Knight GJ, Haddow JE (1983) Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemia. N Engl J Med 308:1265–1267
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