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

Autor:	Simone Iwabe, Gustavo D. Aguirre, Rueben G. Das, Keiko Miyadera, Felipe Pompeo Marinho, Evelyn Santana, Kendra McDaid
Jazyk:	angličtina
Rok vydání:	2018
Předmět:	Male Multifactorial Inheritance Pathology medicine.medical_specialty lcsh:Medicine Retina 03 medical and health sciences Dogs 0302 clinical medicine Retinal Rod Photoreceptor Cells Electroretinography medicine Animals RNA Messenger Author Correction Eye Proteins Cone-Rod Dystrophy lcsh:Science 030304 developmental biology 0303 health sciences Multidisciplinary Behavior Animal business.industry lcsh:R Rod Opsins Dendrites Retinal Photoreceptor Cell Outer Segment Pedigree Disease Models Animal Protein Transport Gene Expression Regulation Retinal Cone Photoreceptor Cells Etiology ComputingMethodologies_DOCUMENTANDTEXTPROCESSING Female Retinal function lcsh:Q business Canine model Cone-Rod Dystrophies 030217 neurology & neurosurgery
Zdroj:	Scientific Reports, Vol 8, Iss 1, Pp 1-1 (2018) Scientific Reports
ISSN:	2045-2322
Popis:	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
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bcc99b4ab585f6fe009a08c31790060 http://link.springer.com/article/10.1038/s41598-018-31337-1 Zobrazit plný text záznamu Plný text ve formátu PDF