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Mutations and phenotype in isolated glycerol kinase deficiency.

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Chicago
WALKER, AP, F MUSCATELLI, AN STAFFORD, J CHELLY, N DAHL, HK BLOMQUIST, Joris Delanghe, PJ WILLEMS, B STEINMANN, and AP MONACO. 1996. “Mutations and Phenotype in Isolated Glycerol Kinase Deficiency.” American Journal of Human Genetics 58 (6): 1205–1211.
APA
WALKER, A., MUSCATELLI, F., STAFFORD, A., CHELLY, J., DAHL, N., BLOMQUIST, H., Delanghe, J., et al. (1996). Mutations and phenotype in isolated glycerol kinase deficiency. AMERICAN JOURNAL OF HUMAN GENETICS, 58(6), 1205–1211.
Vancouver
1.
WALKER A, MUSCATELLI F, STAFFORD A, CHELLY J, DAHL N, BLOMQUIST H, et al. Mutations and phenotype in isolated glycerol kinase deficiency. AMERICAN JOURNAL OF HUMAN GENETICS. 1996;58(6):1205–11.
MLA
WALKER, AP, F MUSCATELLI, AN STAFFORD, et al. “Mutations and Phenotype in Isolated Glycerol Kinase Deficiency.” AMERICAN JOURNAL OF HUMAN GENETICS 58.6 (1996): 1205–1211. Print.
@article{188263,
  author       = {WALKER, AP and MUSCATELLI, F and STAFFORD, AN and CHELLY, J and DAHL, N and BLOMQUIST, HK and Delanghe, Joris and WILLEMS, PJ and STEINMANN, B and MONACO, AP},
  issn         = {0002-9297},
  journal      = {AMERICAN JOURNAL OF HUMAN GENETICS},
  language     = {eng},
  number       = {6},
  pages        = {1205--1211},
  title        = {Mutations and phenotype in isolated glycerol kinase deficiency.},
  volume       = {58},
  year         = {1996},
}