pmc logo image
Logo of ajhgJournal URL: http://www.cell.com/AJHG/
Journal List > Am J Hum Genet > v.25(3); May 1973

Formats:
Am J Hum Genet. 1973 May; 25(3): 294–301.
PMCID: PMC1762530
Copyright notice
Electrophoretic and kinetic studies of glucosephosphate isomerase (GPI) in two different Japanese families with GPI deficiency.
K Nakashima, S Miwa, S Oda, E Oda, and N Matsumoto
Small right arrow pointing to: This article has been cited by other articles in PMC.
Full text
Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (1007K), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.
 
icon of scanned page 294
294
icon of scanned page 295
295
icon of scanned page 296
296
icon of scanned page 297
297
icon of scanned page 298
298
icon of scanned page 299
299
icon of scanned page 300
300
icon of scanned page 301
301
 
Images in this article
Fig. 2
Fig. 2

Fig. 2
on p.297
Fig. 3
Fig. 3

Fig. 3
on p.297
Fig. 4
Fig. 4

Fig. 4
on p.298
Fig. 5
Fig. 5

Fig. 5
on p.298
Click on the image to see a larger version.
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
  • Baughan MA, Valentine WN, Paglia DE, Ways PO, Simons ER, DeMarsh QB. Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes. Blood. 1968 Aug;32(2):236–249. [PubMed]
  • Paglia DE, Holland P, Baughan MA, Valentine WN. Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes. N Engl J Med. 1969 Jan 9;280(2):66–71. [PubMed]
  • Arnold H, Blume KG, Busch D, Lenkeit U, Löhr GW, Lübs E. Klinische und biochemische Untersuchungen zur Glucosephosphatisomerase normaler menschlicher Erythrocyten und bei Glucosephosphatisomerase-Mangel. Klin Wochenschr. 1970 Nov 1;48(21):1299–1308. [PubMed]
  • Schröter W, Brittinger G, Zimmerschmitt E, König E, Schrader D. Combined glucosephosphate isomerase and glucose-6-phosphate dehydrogenase deficiency of the erythrocytes: a new haemolytic syndrome. Br J Haematol. 1971 Mar;20(3):249–261. [PubMed]
  • Blume KG, Hryniuk W, Powars D, Trinidad F, West C, Beutler E. Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia. J Lab Clin Med. 1972 Jun;79(6):942–949. [PubMed]
  • Detter JC, Ways PO, Giblett ER, Baughan MA, Hopkinson DA, Povey S, Harris H. Inherited variations in human phosphohexose isomerase. Ann Hum Genet. 1968 May;31(4):329–338. [PubMed]
  • Carter ND, Yoshida A. Purification and characterization of human phosphoglucose isomerase. Biochim Biophys Acta. 1969 May;181(1):12–19. [PubMed]
  • Dacie JV, Shinton NK, Gaffney PJ, Jr, Lehmann H. Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser). Nature. 1967 Nov 18;216(5116):663–665. [PubMed]
Articles from American Journal of Human Genetics are provided here courtesy of
American Society of Human Genetics

PubMed articles by these authors