Ghent University Academic Bibliography

Advanced

New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations

Bert Callewaert UGent, Marjolijn Renard UGent, Vishwanathan Hucthagowder, Beate Albrecht, Ingrid Hausser, Edward Blair, Cristina Dias, Alice Albino, Hiroshi Wachi and Fumiaki Sato, et al. (2011) HUMAN MUTATION. 32(4). p.445-455
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
MARFAN-SYNDROME, MISSENSE MUTATION, OCCIPITAL HORN SYNDROME, ELASTIC FIBER FORMATION, EXTRACELLULAR-MATRIX, TERMINAL DOMAIN, BINDING PROTEIN, TROPOELASTIN, GENE, FORM, ELN, CL, connective tissue, skin, aneurysm, emphysema
journal title
HUMAN MUTATION
Hum. Mutat.
volume
32
issue
4
pages
445 - 455
Web of Science type
Article
Web of Science id
000288464100017
JCR category
GENETICS & HEREDITY
JCR impact factor
5.686 (2011)
JCR rank
19/155 (2011)
JCR quartile
1 (2011)
ISSN
1059-7794
DOI
10.1002/humu.21462
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
1860451
handle
http://hdl.handle.net/1854/LU-1860451
date created
2011-07-20 14:08:57
date last changed
2011-07-29 15:24:07
@article{1860451,
  author       = {Callewaert, Bert and Renard, Marjolijn and Hucthagowder, Vishwanathan and Albrecht, Beate and Hausser, Ingrid and Blair, Edward and Dias, Cristina and Albino, Alice and Wachi, Hiroshi and Sato, Fumiaki and Mecham, Robert P and Loeys, Bart and Coucke, Paul and De Paepe, Anne and Urban, Zsolt},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  keyword      = {MARFAN-SYNDROME,MISSENSE MUTATION,OCCIPITAL HORN SYNDROME,ELASTIC FIBER FORMATION,EXTRACELLULAR-MATRIX,TERMINAL DOMAIN,BINDING PROTEIN,TROPOELASTIN,GENE,FORM,ELN,CL,connective tissue,skin,aneurysm,emphysema},
  language     = {eng},
  number       = {4},
  pages        = {445--455},
  title        = {New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations},
  url          = {http://dx.doi.org/10.1002/humu.21462},
  volume       = {32},
  year         = {2011},
}

Chicago
Callewaert, Bert, Marjolijn Renard, Vishwanathan Hucthagowder, Beate Albrecht, Ingrid Hausser, Edward Blair, Cristina Dias, et al. 2011. “New Insights into the Pathogenesis of Autosomal-dominant Cutis Laxa with Report of Five ELN Mutations.” Human Mutation 32 (4): 445–455.
APA
Callewaert, B., Renard, M., Hucthagowder, V., Albrecht, B., Hausser, I., Blair, E., Dias, C., et al. (2011). New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations. HUMAN MUTATION, 32(4), 445–455.
Vancouver
1.
Callewaert B, Renard M, Hucthagowder V, Albrecht B, Hausser I, Blair E, et al. New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations. HUMAN MUTATION. 2011;32(4):445–55.
MLA
Callewaert, Bert, Marjolijn Renard, Vishwanathan Hucthagowder, et al. “New Insights into the Pathogenesis of Autosomal-dominant Cutis Laxa with Report of Five ELN Mutations.” HUMAN MUTATION 32.4 (2011): 445–455. Print.