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Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome

Brian P Kelley, Fransiska Malfait UGent, Luisa Bonafe, Dustin Baldridge, Erica Homan, Sofie Symoens UGent, Andy Willaert UGent, Nursel Elcioglu, Lionel Van Maldergem, Christine Verellen-Dumoulin, et al. (2011) JOURNAL OF BONE AND MINERAL RESEARCH. 26(3). p.666-672
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
BRUCK SYNDROME, FKBP10 (ALSO KNOWN AS FKBP65), OSTEOGENESIS IMPERFECTA, BRITTLE BONE DISEASE, COLLAGEN, CONGENITAL JOINT CONTRACTURES, TELOPEPTIDE LYSYL HYDROXYLASE, FK506-BINDING PROTEIN, CROSS-LINKING, ENDOPLASMIC-RETICULUM, BONE FRAGILITY, I COLLAGEN, IDENTIFICATION, CARTILAGE, ELASTIN
journal title
JOURNAL OF BONE AND MINERAL RESEARCH
J. Bone Miner. Res.
volume
26
issue
3
pages
666 - 672
Web of Science type
Article
Web of Science id
000287827600026
JCR category
ENDOCRINOLOGY & METABOLISM
JCR impact factor
6.373 (2011)
JCR rank
13/121 (2011)
JCR quartile
1 (2011)
ISSN
0884-0431
DOI
10.1002/jbmr.250
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
1199054
handle
http://hdl.handle.net/1854/LU-1199054
date created
2011-03-30 11:28:12
date last changed
2016-12-19 15:45:12
@article{1199054,
  author       = {Kelley, Brian P and Malfait, Fransiska and Bonafe, Luisa and Baldridge, Dustin and Homan, Erica and Symoens, Sofie and Willaert, Andy and Elcioglu, Nursel and Van Maldergem, Lionel and Verellen-Dumoulin, Christine and Gillerot, Yves and Napierala, Dobrawa and Krakow, Deborah and Beighton, Peter and Superti-Furga, Andrea and De Paepe, Anne and Lee, Brendan},
  issn         = {0884-0431},
  journal      = {JOURNAL OF BONE AND MINERAL RESEARCH},
  keyword      = {BRUCK SYNDROME,FKBP10 (ALSO KNOWN AS FKBP65),OSTEOGENESIS IMPERFECTA,BRITTLE BONE DISEASE,COLLAGEN,CONGENITAL JOINT CONTRACTURES,TELOPEPTIDE LYSYL HYDROXYLASE,FK506-BINDING PROTEIN,CROSS-LINKING,ENDOPLASMIC-RETICULUM,BONE FRAGILITY,I COLLAGEN,IDENTIFICATION,CARTILAGE,ELASTIN},
  language     = {eng},
  number       = {3},
  pages        = {666--672},
  title        = {Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome},
  url          = {http://dx.doi.org/10.1002/jbmr.250},
  volume       = {26},
  year         = {2011},
}

Chicago
Kelley, Brian P, Fransiska Malfait, Luisa Bonafe, Dustin Baldridge, Erica Homan, Sofie Symoens, Andy Willaert, et al. 2011. “Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome.” Journal of Bone and Mineral Research 26 (3): 666–672.
APA
Kelley, B. P., Malfait, F., Bonafe, L., Baldridge, D., Homan, E., Symoens, S., Willaert, A., et al. (2011). Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome. JOURNAL OF BONE AND MINERAL RESEARCH, 26(3), 666–672.
Vancouver
1.
Kelley BP, Malfait F, Bonafe L, Baldridge D, Homan E, Symoens S, et al. Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome. JOURNAL OF BONE AND MINERAL RESEARCH. 2011;26(3):666–72.
MLA
Kelley, Brian P, Fransiska Malfait, Luisa Bonafe, et al. “Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome.” JOURNAL OF BONE AND MINERAL RESEARCH 26.3 (2011): 666–672. Print.