TY  - GEN
AU  - Manes,Gaël
AU  - Cheguru,Pallavi
AU  - Majumder,Anurima
AU  - Bocquet,Béatrice
AU  - Sénéchal,Audrey
AU  - Artemyev,Nikolai O
AU  - Hamel,Christian P
AU  - Brabet,Philippe
TI  - A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit
SN  - 1932-6203
PY  - 2015///0109
KW  - Animals
KW  - Animals, Genetically Modified
KW  - Catalytic Domain
KW  - genetics
KW  - Cyclic Nucleotide Phosphodiesterases, Type 6
KW  - Eye Diseases, Hereditary
KW  - etiology
KW  - Genetic Diseases, X-Linked
KW  - Heterotrimeric GTP-Binding Proteins
KW  - Humans
KW  - Light Signal Transduction
KW  - Mutation
KW  - Myopia
KW  - Night Blindness
KW  - Transducin
KW  - Xenopus laevis
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1371/journal.pone.0095768
ER  -