C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations
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 AVolume:
58
Language:
english
Journal:
Investigative Opthalmology & Visual Science
DOI:
10.1167/iovs.17-21597
Date:
August, 2017
File:
PDF, 847 KB
english, 2017