[Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study]
- PMID: 5425825
[Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study]
Similar articles
-
[The activity of the enzyme galactokinase in the erythrocytes of healthy children and adults (author's transl)].Klin Padiatr. 1973 Nov;185(6):444-8. Klin Padiatr. 1973. PMID: 4361008 German. No abstract available.
-
Hereditary galactokinase deficiency.Arch Dis Child. 1971 Aug;46(248):465-9. doi: 10.1136/adc.46.248.465. Arch Dis Child. 1971. PMID: 5109408 Free PMC article.
-
Galactokinase deficiency as a cause of cataracts.N Engl J Med. 1973 Jun 7;288(23):1203-6. doi: 10.1056/NEJM197306072882303. N Engl J Med. 1973. PMID: 4700553 No abstract available.
-
The inherited defects of erythrocyte metabolism.Ital J Biochem. 1969 Jul-Aug;18(4):185-326. Ital J Biochem. 1969. PMID: 4243574 Review. No abstract available.
-
[Galactokinase deficiency].Ann Pediatr (Paris). 1976 May 2;23(5):371-7. Ann Pediatr (Paris). 1976. PMID: 16104211 Review. French. No abstract available.
Cited by
-
Clinical features of galactokinase deficiency: a review of the literature.J Inherit Metab Dis. 2002 Dec;25(8):629-34. doi: 10.1023/a:1022875629436. J Inherit Metab Dis. 2002. PMID: 12705493 Review.
-
Galactokinase deficiency in a newborn infant.Arch Dis Child. 1971 Dec;46(250):864-6. doi: 10.1136/adc.46.250.864. Arch Dis Child. 1971. PMID: 5129188 Free PMC article. No abstract available.
MeSH terms
Substances
LinkOut - more resources
Medical