TY  - GEN
AU  - Schorderet,Daniel F
AU  - Escher,Pascal
TI  - NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)
SN  - 1098-1004
PY  - 2010///0225
KW  - Animals
KW  - Databases, Genetic
KW  - Diagnosis, Differential
KW  - Eye Diseases, Hereditary
KW  - diagnosis
KW  - Genotype
KW  - Humans
KW  - Mice
KW  - Mutation
KW  - Orphan Nuclear Receptors
KW  - chemistry
KW  - Retinitis Pigmentosa
KW  - genetics
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1002/humu.21096
ER  -