TY  - GEN
AU  - Libby,R T
AU  - Steel,K P
TI  - Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B
SN  - 0146-0404
PY  - 2001///0315
KW  - Aging
KW  - Animals
KW  - Dark Adaptation
KW  - Deafness
KW  - genetics
KW  - Dyneins
KW  - Electroretinography
KW  - Female
KW  - Male
KW  - Mice
KW  - Mice, Inbred BALB C
KW  - Mice, Inbred C3H
KW  - Mice, Inbred C57BL
KW  - Mice, Inbred CBA
KW  - Mice, Mutant Strains
KW  - Mutation
KW  - Myosin VIIa
KW  - Myosins
KW  - Retina
KW  - physiopathology
KW  - Retinal Degeneration
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
ER  -