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Mutations and phenotype in isolated glycerol kinase deficiency.

AP WALKER, F MUSCATELLI, AN STAFFORD, J CHELLY, N DAHL, HK BLOMQUIST, Joris Delanghe UGent, PJ WILLEMS, B STEINMANN and AP MONACO (1996) AMERICAN JOURNAL OF HUMAN GENETICS. 58(6). p.1205-1211
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
journal title
AMERICAN JOURNAL OF HUMAN GENETICS
Am. J. Hum. Genet.
volume
58
issue
6
pages
1205-1211 pages
Web of Science type
Article
ISSN
0002-9297
language
English
UGent publication?
yes
classification
A1
id
188263
handle
http://hdl.handle.net/1854/LU-188263
date created
2004-01-14 13:41:00
date last changed
2016-12-19 15:39:01
@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},
}

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.