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收藏CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
Kohl, S; Varsanyi, B; Antunes, GA; Baumann, B; Hoyng, CB; Jägle, H; Rosenberg, T; Kellner, U; Lorenz, B; Salati, R; Jurklies, B; Farkas, A; Andreasson, S; Weleber, RG; Jacobson, SG; Rudolph, G; Castellan, C; Dollfus, H; Legius, E; Anastasi, M; Bitoun, P; Lev, D; Sieving, PA; Munier, FL; Zrenner, E; Sharpe, LT; Cremers, FPM; Wissinger, B
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收藏CNGA3 mutations in hereditary cone photoreceptor disorders
Wissinger, B; Gamer, D; Jägle, H; Giorda, R; Marx, T; Mayer, S; Tippmann, S; Broghammer, M; Jurklies, B; Rosenberg, T; Jacobson, SG; Sener, EC; Tatlipinar, S; Hoyng, CB; Castellan, C; Bitoun, P; Andreasson, S; Rudolph, G; Kellner, U; Lorenz, B; Wolff, G; Verellen-Dumoulin, C; Schwartz, M; Cremers, FPM; Apfelstedt-ylla, E; Zrenner, E; Salati, R; Sharpe, LT; Kohl, S
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收藏Human rod monochromacy:: Linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11
Wissinger, B; Jägle, H; Kohl, S; Broghammer, M; Baumann, B; Hanna, DB; Hedels, C; Apfelstedt-Sylla, E; Randazzo, G; Jacobson, SG; Zrenner, E; Sharpe, LT
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