Author:
Beck B.,Christensen E.,Brandt N. J.,Pedersen M.
Subject
Genetics (clinical),Genetics
Reference9 articles.
1. Arakawa, T., Ohara, K., Kudo, Z., Tada, K., Hayashi, T. and Mizuno, T. Hyperfolic-acidemia with formiminoglutamic-aciduria following histidine loading.Tohoku J. Exp. Med. 80 (1963) 370–382
2. Arakawa, T., Ohara, K., Takahashi, Y., Ogasawara, J., Hayashi, T., Chiba, R., Wada, Y., Tada, K., Mizuno, T., Okamura, T. and Yoshida, T. Formiminotransferase-deficiency syndrome: a new inborn error of folic acid metabolism.Ann. Paediatr. 205 (1965) 1–11
3. Arakawa, T., Tamura, T., Higashi, O., Ohara, K., Tanno, K., Honda, Y., Narisawa, K., Konno, T., Wada, Y., Sato, Y. and Mizuno, T. Formiminotransferase deficiency syndrome associated with megaloblastic anemia responsive to pyridoxine or folic acid.Tohoku J. Exp. Med. 94 (1968a) 2–16
4. Arakawa, T., Tamura, T., Ohara, K., Narisawa, K., Tanno, K., Honda, Y. and Higashi, O. Familial occurrence of formiminotransferase deficiency syndrome.Tohoku J. Exp. Med. 96 (1968b) 211–217
5. Arakawa, T., Yoshida, T., Konno, T. and Honda, Y. Defect of incorporation of glycine-l-14C into urinary uric acid in formiminotransferase deficiency syndrome.Tohoku J. Exp. Med. 106 (1972) 213–218
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