TY  - GEN
AU  - Chassine,Thomas
AU  - Bocquet,Béatrice
AU  - Daien,Vincent
AU  - Avila-Fernandez,Almudena
AU  - Ayuso,Carmen
AU  - Collin,Rob Wj
AU  - Corton,Marta
AU  - Hejtmancik,J Fielding
AU  - van den Born,L Ingeborgh
AU  - Klevering,B Jeroen
AU  - Riazuddin,S Amer
AU  - Sendon,Nathacha
AU  - Lacroux,Annie
AU  - Meunier,Isabelle
AU  - Hamel,Christian P
TI  - Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia
SN  - 1468-2079
PY  - 2015///1217
KW  - Adult
KW  - DNA
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Electroretinography
KW  - Eye Proteins
KW  - Female
KW  - Humans
KW  - Male
KW  - Microtubule-Associated Proteins
KW  - Middle Aged
KW  - Mutation
KW  - Myopia
KW  - etiology
KW  - Pedigree
KW  - Phenotype
KW  - Retinitis Pigmentosa
KW  - complications
KW  - Visual Acuity
KW  - Visual Fields
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/bjophthalmol-2014-306224
ER  -