Identification of mutations in <i>CACNA1F</i> in patients with incomplete CSNB applying next generation sequencing approaches - Forschungsportal der Justus-Liebig-Universität Gießen:

Meeting Abstract

Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches

Autorenliste: Zeitz, Christina; Michiels, Christelle; Neuille, Marion; Friedburg, Christoph; Condroyer, Christel; Boyard, Fiona; Antonio, Aline; Preising, Markus N.; Meyer, Vincent; Boland, Anne; Deleuze, Jean-Francois; Mesrob, Lilia; Jurklies, Bernhard; Lorenz, Birgit; Sahel, Jose Alain; Audo, Isabelle S.

Jahr der Veröffentlichung: 2017

Zeitschrift: Investigative Ophthalmology & Visual Science

Bandnummer: 58

Heftnummer: 8

ISSN: 0146-0404

eISSN: 1552-5783

Konferenz: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology (ARVO) - Imaging in the Eye

Verlag: Association for Research in Vision and Ophthalmology

Zitierstile

Harvard-Zitierstil: Zeitz, C., Michiels, C., Neuille, M., Friedburg, C., Condroyer, C., Boyard, F., et al. (2017) Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches, Investigative Ophthalmology & Visual Science, 58(8)

APA-Zitierstil: Zeitz, C., Michiels, C., Neuille, M., Friedburg, C., Condroyer, C., Boyard, F., Antonio, A., Preising, M., Meyer, V., Boland, A., Deleuze, J., Mesrob, L., Jurklies, B., Lorenz, B., Sahel, J., & Audo, I. (2017). Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches. Investigative Ophthalmology & Visual Science. 58(8).