Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
NA Kahle, T Peters, D Zobor, L Kuehlewein… - Human Gene …, 2018 - liebertpub.com
Achromatopsia is an autosomal recessively inherited congenital defect characterized by a
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV. hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
NA Kahle, T Peters, D Zobor, L Kuehlewein… - Human Gene therapy …, 2018 - europepmc.org
Achromatopsia is an autosomal recessively inherited congenital defect characterized by a
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
[引用][C] Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV. hCNGA3 in Patients with CNGA3-Linked …
NA Kahle, T Peters, D Zobor… - Human Gene …, 2018 - ub01.uni-tuebingen.de
Development of Methodology and Study Protocol : Safety and Efficacy of a Single
Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV. hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
NA Kahle, T Peters, D Zobor… - Human gene …, 2018 - pubmed.ncbi.nlm.nih.gov
Achromatopsia is an autosomal recessively inherited congenital defect characterized by a
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
[引用][C] Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV. hCNGA3 in Patients with CNGA3-Linked …
NA Kahle, T Peters, D Zobor… - Human Gene …, 2018 - tobias-lib.ub.uni-tuebingen.de
Development of Methodology and Study Protocol : Safety and Efficacy of a Single
Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV. hCNGA3 in Patients with CNGA3-Linked Achromatopsia …
NA Kahle, T Peters, D Zobor… - Human Gene …, 2018 - epub.ub.uni-muenchen.de
Achromatopsia is an autosomal recessively inherited congenital defect characterized by a
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …
lack of cone photoreceptor function, leading to severely impaired vision. In this clinical study …