C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.

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@article{GerthKahlert2017C2orf71MA, title={C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.}, author={Christina Gerth-Kahlert and Amit Mani Kumar Tiwari and James V. M. Hanson and Vaishnavi Batmanabane and Elias I. Traboulsi and Mark E. Pennesi and Abdullah Aoun Al-Qahtani and Byron L. Lam and John R. Heckenlively and Sandrine A Zweifel and Ajoy Vincent and Fabienne Fierz and D. Barthelmes and Kari E. H. Branham and Naheed Wali Khan and Angela Bahr and Luzy Baehr and Istv{\'a}n Magyar and Samuel Koller and Silvia Azzarello-Burri and Dunja Niedrist and Elise Heon and Wolfgang Berger}, journal={Investigative ophthalmology & visual science}, year={2017}, volume={58 10}, pages={3840-3850} }