Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function-Reference-Cited by-同舟云学术

Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function

Published:2010-12 Issue:12 Volume:18 Page:2057-2063
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Michalakis Stylianos,Mühlfriedel Regine,Tanimoto Naoyuki,Krishnamoorthy Vidhyasankar,Koch Susanne,Fischer M Dominik,Becirovic Elvir,Bai Lin,Huber Gesine,Beck Susanne C,Fahl Edda,Büning Hildegard,Paquet-Durand François,Zong Xiangang,Gollisch Tim,Biel Martin,Seeliger Mathias W

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

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4. The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes;Jagla;Hum Mol Genet,2002

5. Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel;Kohl;Nat Genet,1998

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