» Articles » PMID: 4906700

Genetical Theory and the "inborn Errors of Metabolism"

Overview
Journal Br Med J
Specialty General Medicine
Date 1970 Feb 7
PMID 4906700
Citations 3
Authors
Affiliations
Soon will be listed here.
Citing Articles

Genetics and clinical enzymology.

Harris H J Clin Pathol Suppl (Assoc Clin Pathol). 1970; 4:85-9.

PMID: 4949711 PMC: 1176290. DOI: 10.1136/jcp.s1-4.1.85.


Inheritance of type 2 Crigler-Najjar hyperbilirubinaemia.

Hunter J, Thompson R, Dunn P, Williams R Gut. 1973; 14(1):46-9.

PMID: 4692254 PMC: 1412576. DOI: 10.1136/gut.14.1.46.


Pancreatic alkaline phosphatase and a tumour variant.

Warnes T, Timperley W, Hine P, Kay G Gut. 1972; 13(7):513-9.

PMID: 4341740 PMC: 1412273. DOI: 10.1136/gut.13.7.513.

References
1.
ROSENBERG L, Lilljeqvist A, HSIA Y . Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia. N Engl J Med. 1968; 278(24):1319-22. DOI: 10.1056/NEJM196806132782404. View

2.
Kelley W, Rosenbloom F, HENDERSON J, Seegmiller J . A specific enzyme defect in gout associated with overproduction of uric acid. Proc Natl Acad Sci U S A. 1967; 57(6):1735-9. PMC: 224540. DOI: 10.1073/pnas.57.6.1735. View

3.
Oberholzer V, Levin B, Burgess E, Young W . Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis. Arch Dis Child. 1967; 42(225):492-504. PMC: 2019805. DOI: 10.1136/adc.42.225.492. View

4.
La Du B, Zannoni V, LASTER L, Seegmiller J . The nature of the defect in tyrosine metabolism in alcaptonuria. J Biol Chem. 1958; 230(1):251-60. View

5.
Yoshida A, Stamatoyannopoulos G, Motulsky A . Negro variant of glucose-6-phosphate dehydrogenase deficiency (A-) in man. Science. 1967; 155(3758):97-9. DOI: 10.1126/science.155.3758.97. View