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Progression of Vision Loss in Macular Telangiectasia Type 2.
Heeren TF, Clemons T, Scholl HP, Bird AC, Holz FG, Charbel Issa P. Heeren TF, et al. Among authors: scholl hp. Invest Ophthalmol Vis Sci. 2015 Jun;56(6):3905-12. doi: 10.1167/iovs.15-16915. Invest Ophthalmol Vis Sci. 2015. PMID: 26070062
Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy.
Khan KN, El-Asrag ME, Ku CA, Holder GE, McKibbin M, Arno G, Poulter JA, Carss K, Bommireddy T, Bagheri S, Bakall B, Scholl HP, Raymond FL, Toomes C, Inglehearn CF, Pennesi ME, Moore AT, Michaelides M, Webster AR, Ali M; for NIHR BioResource-Rare Diseases and UK Inherited Retinal Disease Consortium. Khan KN, et al. Among authors: scholl hp. Invest Ophthalmol Vis Sci. 2017 Jun 1;58(7):2906-2914. doi: 10.1167/iovs.16-20608. Invest Ophthalmol Vis Sci. 2017. PMID: 28586915 Free article.
325 results