Publication: C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations
C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations
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Gerth-Kahlert, C., Tiwari, A., Hanson, J. V. M., Batmanabane, V., Traboulsi, E., Pennesi, M. E., Al-Qahtani, A. A., Lam, B. L., Heckenlively, J., Zweifel, S. A., Vincent, A., Fierz, F., Barthelmes, D., Branham, K., Khan, N., Bahr, A., Baehr, L., Magyar, I., Koller, S., … Berger, W. (2017). C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. Investigative Ophthalmology & Visual Science, 58(10), 3840–3850. https://doi.org/10.1167/iovs.17-21597
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Creators (Authors)
- Gerth-Kahlert, Christina
- Tiwari, Amit
- Hanson, James V M
- Batmanabane, Vaishnavi
- Traboulsi, Elias
- Pennesi, Mark E
- Al-Qahtani, Abdullah A
- Lam, Byron L
- Heckenlively, John
- Zweifel, Sandrine A
- Vincent, Ajoy
- Fierz, Fabienne
- Barthelmes, Daniel
- Branham, Kari
- Khan, Naheed
- Baehr, Luzy
- Magyar, István
- Koller, Samuel
- Azzarello-Burri, Silvia
- Heon, Elise
- Berger, Wolfgang
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Gerth-Kahlert, C., Tiwari, A., Hanson, J. V. M., Batmanabane, V., Traboulsi, E., Pennesi, M. E., Al-Qahtani, A. A., Lam, B. L., Heckenlively, J., Zweifel, S. A., Vincent, A., Fierz, F., Barthelmes, D., Branham, K., Khan, N., Bahr, A., Baehr, L., Magyar, I., Koller, S., … Berger, W. (2017). C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. Investigative Ophthalmology & Visual Science, 58(10), 3840–3850. https://doi.org/10.1167/iovs.17-21597
