Author:
Kobayashi Keiko,Itakura Yoshihiro,Saheki Takeyori,Nakano Kyoko,Sase Mariko,Oyanagi Kazuhiko,Okamoto Ryozo,Mino Makoto
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference24 articles.
1. A disease, probably hereditary, characterised by severe mental deficiency and a constant gross abnormality of amino acid metabolism;Allan;Lancet,1958
2. Urea cycle disorders and other congenital hyperammonemic syndromes;Shih,1978
3. Urea cycle disorders and other hereditary hyperammonemic syndromes;Walser,1983
4. First case of argininosuccinic aciduria in Japan: clinical observations and treatment;Sakiyama;Adv Exp Med Biol,1982
5. Argininosuccininic aciduria associated with argininosuccinate synthetase deficiency in liver;Oyanagi;Rinsho-Shoni-Igaku,1985
Cited by
15 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