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Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response

Bernd Wissinger, Simone Schaich, Britta Baumann, Michael Bonin, Herbert Jägle, Christoph Friedburg, Balázs Varsányi, Carel B Hoyng, Hélène Dollfus, John R Heckenliyely, et al. (2011) HUMAN MUTATION. 32(12). p.1398-1406
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
Kv channel, LIPOPROTEIN RECEPTOR GENE, KCNV2, deletion, retinal dystrophy, CEREBELLAR HYPOPLASIA, QUADRUPEDAL LOCOMOTION, ALPHA-SUBUNITS, MUTATIONS, CHANNEL, ELECTRORETINOGRAM, HUMANS, MODEL
journal title
HUMAN MUTATION
Hum. Mutat.
volume
32
issue
12
pages
1398 - 1406
Web of Science type
Article
Web of Science id
000297246800012
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.21580
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
2053881
handle
http://hdl.handle.net/1854/LU-2053881
date created
2012-03-01 09:43:35
date last changed
2016-12-19 15:44:51
@article{2053881,
  author       = {Wissinger, Bernd and Schaich, Simone and Baumann, Britta and Bonin, Michael and J{\"a}gle, Herbert and Friedburg, Christoph and Vars{\'a}nyi, Bal{\'a}zs and Hoyng, Carel B and Dollfus, H{\'e}l{\`e}ne and Heckenliyely, John R and Rosenberg, Thomas and Rudolph, G{\"u}nter and Kellner, Ulrich and Salati, Roberto and Plomp, Astrid and De Baere, Elfride and Andrassi-Darida, Monika and Sauer, Alexandra and Wolf, Christiane and Zobor, Ditta and Bernd, Antje and Leroy, Bart and Enyedi, Peter and Cremers, Frans PM and Lorenz, Birgit and Zrenner, Eberhart and Kohl, Susanne},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  keyword      = {Kv channel,LIPOPROTEIN RECEPTOR GENE,KCNV2,deletion,retinal dystrophy,CEREBELLAR HYPOPLASIA,QUADRUPEDAL LOCOMOTION,ALPHA-SUBUNITS,MUTATIONS,CHANNEL,ELECTRORETINOGRAM,HUMANS,MODEL},
  language     = {eng},
  number       = {12},
  pages        = {1398--1406},
  title        = {Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response},
  url          = {http://dx.doi.org/10.1002/humu.21580},
  volume       = {32},
  year         = {2011},
}

Chicago
Wissinger, Bernd, Simone Schaich, Britta Baumann, Michael Bonin, Herbert Jägle, Christoph Friedburg, Balázs Varsányi, et al. 2011. “Large Deletions of the KCNV2 Gene Are Common in Patients with Cone Dystrophy with Supernormal Rod Response.” Human Mutation 32 (12): 1398–1406.
APA
Wissinger, B., Schaich, S., Baumann, B., Bonin, M., Jägle, H., Friedburg, C., Varsányi, B., et al. (2011). Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. HUMAN MUTATION, 32(12), 1398–1406.
Vancouver
1.
Wissinger B, Schaich S, Baumann B, Bonin M, Jägle H, Friedburg C, et al. Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. HUMAN MUTATION. 2011;32(12):1398–406.
MLA
Wissinger, Bernd, Simone Schaich, Britta Baumann, et al. “Large Deletions of the KCNV2 Gene Are Common in Patients with Cone Dystrophy with Supernormal Rod Response.” HUMAN MUTATION 32.12 (2011): 1398–1406. Print.