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Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome

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Keywords
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

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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.
@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},
}

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