CDHR1 mutations in retinal dystrophies-Reference-Cited by-同舟云学术

CDHR1 mutations in retinal dystrophies

Published:2017-08-01 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Stingl Katarina,Mayer Anja K.,Llavona Pablo,Mulahasanovic Lejla,Rudolph Günther,Jacobson Samuel G.,Zrenner Eberhart,Kohl Susanne^ORCID,Wissinger Bernd,Weisschuh Nicole

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-07117-8.pdf

Reference38 articles.

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2. Michaelides, M., Hardcastle, A. J., Hunt, D. M. & Moore, A. T. Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis. Surv Ophthalmol. 51, 232–258 (2006).

3. Weleber, R. G. Retinitis pigmentosa and allied disorders in Retina (ed. Ryan, S. J.) 335–466 (Mosby, 1994).

4. Nollet, F., Kools, P. & van Roy, F. Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members. J Mol Biol 299, 551–572 (2000).

5. Ahmed, Z. M. et al. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am J Hum Gen 69, 25–34 (2001).

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