Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Sensory Systems,Ophthalmology
Reference42 articles.
1. Anderson, E. P., H. M. Kalckar &K. J. Isselbacher. Defect in uptake of galactose-1-phosphate into liver nucleotides in congenital galactosemia.Science, 125,113–114 (1957).
2. Baker, L., W. J. Mellman, T. A. Tedesco &S. Segal. Galactosemia. Symptomatic and asymptomatic homozygotes in one negro sibship.J. Pediat. 68,551–558 (1966).
3. Beutler, E., M. C. Baluda, P. Sturgeon &R. Day. A new genetic abnormality resulting in galactose-1-phosphate uridyltransferase deficiency.Lancet I,353–354 (1965).
4. — &M. C. Baluda. Improved methods for measuring galactose-1-phosphate uridyltransferase activity of erythrocytes.Clin. chim. Acta, 13,369–379 (1966).
5. — &M. Mitchell. New rapid method for the estimation of red cell galactose-1-phosphate uridyl transferase activity.J. Lab. clin. Med. 72,527–532 (1968).
Cited by
1 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