Author Correction: Variabilities in retinal function and structure in a canine model of cone-rod dystrophy associated with RPGRIP1 support multigenic etiology

Authors :: Simone Iwabe
Gustavo D. Aguirre
Rueben G. Das
Keiko Miyadera
Felipe Pompeo Marinho
Evelyn Santana
Kendra McDaid
Source :: Scientific Reports, Vol 8, Iss 1, Pp 1-1 (2018), Scientific Reports
Publication Year :: 2018
Publisher :: Nature Publishing Group, 2018.
Abstract: Defects in the cilia gene RPGRIP1 cause Leber congenital amaurosis and cone-rod dystrophy in humans. A form of canine cone-rod dystrophy (cord1) was originally associated with a homozygous insertion in RPGRIP1 (RPGRIP1

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