Author:
Tuchman Mendel,Lee Brendan,Lichter-Konecki Uta,Summar Marshall L.,Yudkoff Marc,Cederbaum Stephen D.,Kerr Douglas S.,Diaz George A.,Seashore Margaretta R.,Lee Hye-Seung,McCarter Robert J.,Krischer Jeffrey P.,Batshaw Mark L.
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference15 articles.
1. Rare Diseases Act of 2002 Public Law 107-280 107th Congress. HOUSE Reports: No. 107-543 (Committee on Energy and Commerce). Senate Reports: No. 107-129 accompanying S. 1379 (Committee on Health).
2. Genotype spectrum of ornithine transcarbamylase deficiency: correlation with the clinical and biochemical phenotype;McCullough;Am. J. Med. Genet.,2000
3. Anonymous, Progress against childhood cancer: the pediatric oncology group experience, Pediatrics 89 (4 Pt. 1) (1992) 597–600.
4. Estimated frequency of urea cycle enzymopathies in Japan;Nagata;Am. J. Med. Genet.,1991
5. Urea cycle disorders: diagnosis, pathophysiology, therapy;Brusilow,1996
Cited by
177 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