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pro vyhledávání: '"Nadine Hemmrich"'
Autor:
Bernhard H. F. Weber, Heidi Stöhr, Karen White, Nadine Hemmrich, Hendrik P. N. Scholl, Klaus Steiner, Bernhard Jurklies, T. Grimm, Eckhart Apfelstedt-Sylla, Birgit Lorenz, Andrea Rivera
Publikováno v:
The American Journal of Human Genetics. (4):800-813
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 photoreceptor-specific ATP-binding cassette (ABC) transporter (ABCA4). We have studied 144 patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98d4b1007a26063503cd3b9b3970f70
