Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.

Libby, R T

Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B. [electronic resource] - Investigative ophthalmology & visual science Mar 2001 - 770-8 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0146-0404


Aging
Animals
Dark Adaptation
Deafness--genetics
Dyneins
Electroretinography
Female
Male
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Mice, Inbred C57BL
Mice, Inbred CBA
Mice, Mutant Strains
Mutation
Myosin VIIa
Myosins--genetics
Retina--physiopathology
Retinal Degeneration--genetics
Syndrome