Diagnosis and treatment of urea cycle disorder in Japan
Author:
Affiliation:
1. Department of Pediatrics; Kumamoto University Hospital; Kumamoto Japan
2. Department of Neonatology; Kumamoto University Hospital; Kumamoto Japan
Funder
Ministry of Health and Welfare
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12439/fullpdf
Reference24 articles.
1. Clinical manifestation of inborn errors of urea cycle and related metabolic disorders during childhood;Endo;J. Nutr.,2004
2. Estimated frequency of urea cycle enzymopathies in Japan;Nagata;Am. J. Med. Genet.,1991
3. The ornithine transcarbamylase (OTC) gene: Mutations in 50 Japanese families with OTC deficiency;Matsuda;Am. J. Med. Genet.,1997
4. Outcome and survival of 88 patients with urea cycle disorders: A retrospective evaluation;Bachmann;Eur. J. Pediatr.,2003
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