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. 1967 Sep 23;97(13):773–779.

Familial chronic acidosis due to an error in lactate and pyruvate metabolism.

J C Haworth, J D Ford, M K Younoszai

PMCID: PMC1923319 PMID: 6050895

779

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

ERICKSON R. J. FAMILIAL INFANTILE LACTIC ACIDOSIS. J Pediatr. 1965 Jun;66:1004–1016. doi: 10.1016/s0022-3476(65)80085-3. [DOI] [PubMed] [Google Scholar]
HARTMANN A. F., Sr, WOHLTMANN H. J., PURKERSON M. L., WESLEY M. E. Lactate metabolism. Studies of a child with a serious congenital deviation. J Pediatr. 1962 Aug;61:165–180. doi: 10.1016/s0022-3476(62)80251-0. [DOI] [PubMed] [Google Scholar]
Worsley H. E., Brookfield R. W., Elwood J. S., Noble R. L., Taylor W. H. Lactic acidosis with necrotizing encephalopathy in two sibs. Arch Dis Child. 1965 Oct;40(213):492–501. doi: 10.1136/adc.40.213.492. [DOI] [PMC free article] [PubMed] [Google Scholar]
ZELNICEK E., MRSKOS A., KRYSTIK F. THE METABOLISM OF ALPHA-KETO ACIDS IN VON GIERKE'S DISEASE. Clin Chim Acta. 1964 Jun;9:587–589. doi: 10.1016/0009-8981(64)90127-5. [DOI] [PubMed] [Google Scholar]
Zinkham W. H., Blanco A., Kupchyk L. Isozymes: biological and clinical significance. Pediatrics. 1966 Jan;37(1):120–131. [PubMed] [Google Scholar]

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