Advanced search

Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria.

(1996) KIDNEY INTERNATIONAL. 50(5). p.1747-1752
Author
Organization

Citation

Please use this url to cite or link to this publication:

Chicago
VANACKER, KJ, FJ EYSKENS, Marc Espeel, RJA WANDERS, C DEKKER, Ingrid Kerckaert, and Frank Roels. 1996. “Hyperoxaluria with Hyperglycoluria Not Due to Alanine:glyoxylate Aminotransferase Defect: A Novel Type of Primary Hyperoxaluria.” Kidney International 50 (5): 1747–1752.
APA
VANACKER, K., EYSKENS, F., Espeel, M., WANDERS, R., DEKKER, C., Kerckaert, I., & Roels, F. (1996). Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria. KIDNEY INTERNATIONAL, 50(5), 1747–1752.
Vancouver
1.
VANACKER K, EYSKENS F, Espeel M, WANDERS R, DEKKER C, Kerckaert I, et al. Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria. KIDNEY INTERNATIONAL. 1996;50(5):1747–52.
MLA
VANACKER, KJ, FJ EYSKENS, Marc Espeel, et al. “Hyperoxaluria with Hyperglycoluria Not Due to Alanine:glyoxylate Aminotransferase Defect: A Novel Type of Primary Hyperoxaluria.” KIDNEY INTERNATIONAL 50.5 (1996): 1747–1752. Print.
@article{190496,
  author       = {VANACKER, KJ and EYSKENS, FJ and Espeel, Marc and WANDERS, RJA and DEKKER, C and Kerckaert, Ingrid and Roels, Frank},
  issn         = {0085-2538},
  journal      = {KIDNEY INTERNATIONAL},
  language     = {eng},
  number       = {5},
  pages        = {1747--1752},
  title        = {Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria.},
  volume       = {50},
  year         = {1996},
}