TY  - GEN
AU  - Scheidecker,Sophie
AU  - Hull,Sarah
AU  - Perdomo,Yaumara
AU  - Studer,Fouzia
AU  - Pelletier,Valérie
AU  - Muller,Jean
AU  - Stoetzel,Corinne
AU  - Schaefer,Elise
AU  - Defoort-Dhellemmes,Sabine
AU  - Drumare,Isabelle
AU  - Holder,Graham E
AU  - Hamel,Christian P
AU  - Webster,Andrew R
AU  - Moore,Anthony T
AU  - Puech,Bernard
AU  - Dollfus,Hélène J
TI  - Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome
SN  - 1879-1891
PY  - 2015///0928
KW  - Adult
KW  - Bardet-Biedl Syndrome
KW  - complications
KW  - DNA
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Electroretinography
KW  - Eye Proteins
KW  - Female
KW  - Fluorescein Angiography
KW  - Fundus Oculi
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Phenotype
KW  - Retinal Cone Photoreceptor Cells
KW  - physiology
KW  - Retinal Degeneration
KW  - etiology
KW  - Retrospective Studies
KW  - Tomography, Optical Coherence
KW  - Visual Acuity
KW  - Visual Fields
N1  - Publication Type: Journal Article; Multicenter Study; Observational Study; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajo.2015.05.007
ER  -