Cirrhosis in an infant heterozygous for classical citrullinaemia
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1080/0803525051003078/fullpdf
Reference12 articles.
1. Treem, W. (2002) Fulminant hepatic failure in children J Pediatr Gastroenterol Nutr, 35, pp. S33 - 8.
2. Burdelski, M and Nolkemper, D and Ganschow, R and Sturm, E and Malago, M and Rogiers, X and (1999) Liver transplantation in children: long-term outcome and quality of life Eur J Pediatr, 158 (Suppl 2), pp. S34 - 42.
3. Tokatlı, A and Coşkun, T and Özalp, İ. (1998) Citrullinemia Clinical experience with 23 cases. Turk J Pediatr, 40, pp. 185 - 93.
4. Vilaseca, M and Kobayashi, K and Briones, P and Lambruschini, N and Campistol, J and Tabata, A and (2001) Phenotype and genotype heterogeneity in Mediterranean citrullinemia Mol Genet Metab, 74, pp. 396 - 8.
5. Gao, H and Kobayashi, K and Tabata, A and Tsuge, H and Iijima, M and Yasuda, T and (2003) Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients Hum Mutat, 22, pp. 24 - 34.
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1. Molecular genetics of citrullinemia types I and II;Clinica Chimica Acta;2014-04
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