Meeting Abstract

PEX6 mutation causing deaf blindness with enamel dysplasia and microcephaly


Authors listBolz, Hanno Joern; Heller, Raoul; Thoenes, Michaela; Nuernberg, Gudrun; Nuernberg, Peter; Karnati, Srikanth; Swan, Daniel; Baumgart-Vogt, Eveline; Zaki, Maha

Publication year2015

JournalInvestigative Ophthalmology & Visual Science

Volume number56

Issue number7

ISSN0146-0404

eISSN1552-5783

ConferenceAnnual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology (ARVO)

PublisherAssociation for Research in Vision and Ophthalmology



Citation Styles

Harvard Citation styleBolz, H., Heller, R., Thoenes, M., Nuernberg, G., Nuernberg, P., Karnati, S., et al. (2015) PEX6 mutation causing deaf blindness with enamel dysplasia and microcephaly, Investigative Ophthalmology & Visual Science, 56(7)

APA Citation styleBolz, H., Heller, R., Thoenes, M., Nuernberg, G., Nuernberg, P., Karnati, S., Swan, D., Baumgart-Vogt, E., & Zaki, M. (2015). PEX6 mutation causing deaf blindness with enamel dysplasia and microcephaly. Investigative Ophthalmology & Visual Science. 56(7).


Last updated on 2025-02-04 at 01:56