Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).

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Neuillé, Marion; El Shamieh, Said; Orhan, Elise; Michiels, Christelle; Antonio, Aline; Lancelot, Marie-Elise; Condroyer, Christel; Bujakowska, Kinga; Poch, Olivier; Sahel, José-Alain; Audo, Isabelle; Zeitz, Christina;
  • Publisher: Public Library of Science (PLoS)
  • Journal: PLoS ONE,volume 9,issue 3 (issn: 1932-6203, eissn: 1932-6203)
  • Publisher copyright policies & self-archiving
  • Related identifiers: doi: 10.1371/journal.pone.0090342, pmc: PMC3943948
  • Subject: Animal Models | Research Article | Molecular Cell Biology | Genetic Mutation | [SDV.GEN]Life Sciences [q-bio]/Genetics | [ SDV.GEN ] Life Sciences [q-bio]/Genetics | Mouse | Genetics | Histology | Ophthalmology | [SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs | Biology | Genetics of Disease | Neuroscience | Gene Function | Medicine | Anatomy and Physiology | Ocular System | Q | [ SDV.MHEP.OS ] Life Sciences [q-bio]/Human health and pathology/Sensory Organs | R | Electrophysiology | Model Organisms | Animal Genetics | Science
    mesheuropmc: genetic structures | sense organs

International audience; Mutations in LRIT3, coding for a Leucine-Rich Repeat, immunoglobulin-like and transmembrane domains 3 protein lead to autosomal recessive complete congenital stationary night blindness (cCSNB). The role of the corresponding protein in the ON-bipo... View more
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