Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence. [electronic resource]
Producer: 20090918Description: 4386-93 p. digitalISSN:- 1552-5783
- Animals
- Child
- Choroid -- pathology
- Diagnostic Imaging -- methods
- Disease Models, Animal
- Fluorescence
- Humans
- Melanosomes -- pathology
- Mice
- Mice, Inbred C57BL
- Microscopy, Confocal
- Middle Aged
- Mutation
- Myosin VIIa
- Myosins -- genetics
- Ophthalmoscopy
- Retinal Pigment Epithelium -- pathology
- Tomography, Optical Coherence
- Usher Syndromes -- diagnosis
- Young Adult
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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