Search Results - "Hemmrich, Nadine"

A Comprehensive Survey of Sequence Variation in the ABCA4 ( ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration by Rivera, Andrea, White, Karen, Stöhr, Heidi, Steiner, Klaus, Hemmrich, Nadine, Grimm, Timo, Jurklies, Bernhard, Lorenz, Birgit, Scholl, Hendrik P.N., Apfelstedt-Sylla, Eckhart, Weber, Bernhard H.F.

“…Stargardt disease (STGD) is a common autosomal recessive maculopathy of early and young-adult onset and is caused by alterations in the gene encoding the…”
Get full text

The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe by Maugeri, Alessandra, Flothmann, Kris, Hemmrich, Nadine, Ingvast, Sofie, Jorge, Paula, Paloma, Eva, Patel, Reshma, Rozet, Jean-Michel, Tammur, Jaana, Testa, Francesco, Balcells, Susana, Bird, Alan C, Brunner, Han G, Hoyng, Carel B, Metspalu, Andres, Simonelli, Francesca, Allikmets, Rando, Bhattacharya, Shomi S, D'Urso, Michele, Gonzàlez-Duarte, Roser, Kaplan, Josseline, te Meerman, Gerard J, Santos, Rosário, Schwartz, Marianne, Van Camp, Guy, Wadelius, Claes, Weber, Bernhard H F, Cremers, Frans P M

“…Inherited retinal dystrophies represent the most important cause of vision impairment in adolescence, affecting approximately 1 out of 3000 individuals…”
Get full text