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

(2011) HUMAN MUTATION. 32(12). p.1398-1406
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Keywords
Kv channel, LIPOPROTEIN RECEPTOR GENE, KCNV2, deletion, retinal dystrophy, CEREBELLAR HYPOPLASIA, QUADRUPEDAL LOCOMOTION, ALPHA-SUBUNITS, MUTATIONS, CHANNEL, ELECTRORETINOGRAM, HUMANS, MODEL

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Citation

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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.
@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},
}

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