Mutations and phenotype in isolated glycerol kinase deficiency.
- Author
- AP WALKER, F MUSCATELLI, AN STAFFORD, J CHELLY, N DAHL, HK BLOMQUIST, Joris Delanghe (UGent) , PJ WILLEMS, B STEINMANN and AP MONACO
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-188263
- 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},
}