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1 Ergebnisse
1
Accessory heterozygous mutations in cone photoreceptor CNGA..:
Burkard, Markus
;
Kohl, Susanne
;
Krätzig, Timm
...
qt3tx4n83z. , 2018
Link:
https://escholarship.org/uc/item/3tx4n83z
RT Journal T1
Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3tx4n83z&Exemplar=1&LAN=DE A1 Burkard, Markus A1 Kohl, Susanne A1 Krätzig, Timm A1 Tanimoto, Naoyuki A1 Brennenstuhl, Christina A1 Bausch, Anne E A1 Junger, Katrin A1 Reuter, Peggy A1 Sothilingam, Vithiyanjali A1 Beck, Susanne C A1 Huber, Gesine A1 Ding, Xi-Qin A1 Mayer, Anja K A1 Baumann, Britta A1 Weisschuh, Nicole A1 Zobor, Ditta A1 Hahn, Gesa-Astrid A1 Kellner, Ulrich A1 Venturelli, Sascha A1 Becirovic, Elvir A1 Issa, Peter Charbel A1 Koenekoop, Robert K A1 Rudolph, Günther A1 Heckenlively, John A1 Sieving, Paul A1 Weleber, Richard G A1 Hamel, Christian A1 Zong, Xiangang A1 Biel, Martin A1 Lukowski, Robert A1 Seeliger, Matthias W A1 Michalakis, Stylianos A1 Wissinger, Bernd A1 Ruth, Peter PB eScholarship, University of California YR 2018 K1 Genetics K1 Neurosciences K1 Brain Disorders K1 Eye Disease and Disorders of Vision K1 Aetiology K1 2.1 Biological and endogenous factors K1 Eye K1 Amino Acid Substitution K1 Animals K1 Color Vision Defects K1 Cyclic Nucleotide-Gated Cation Channels K1 Disease Models K1 Animal K1 HEK293 Cells K1 Heterozygote K1 Humans K1 Ion Channel Gating K1 Mice K1 Transgenic K1 Mutation K1 Missense K1 Retinal Cone Photoreceptor Cells K1 Retinal Diseases K1 Molecular genetics K1 Ophthalmology K1 Retinopathy K1 Medical and Health Sciences K1 Immunology JF qt3tx4n83z LK http://dx.doi.org/https://escholarship.org/uc/item/3tx4n83z DO https://escholarship.org/uc/item/3tx4n83z SF ELIB - SuUB Bremen
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