Selective wavelength pupillometry in Leber hereditary optic neuropathy.
| Data(s) |
2010
|
|---|---|
| Identificador |
https://serval.unil.ch/?id=serval:BIB_1C8BAA9D740E isbn:1442-9071[electronic], 1442-6404[linking] pmid:20447133 doi: isiid:000276949000019 |
| Idioma(s) |
en |
| Fonte |
Clinical and Experimental Ophthalmology, vol. 38, no. 3, pp. 322-324 |
| Palavras-Chave | #Adult; Color Vision; Female; Humans; Light; Mutation; Optic Atrophy, Hereditary, Leber/genetics; Optic Atrophy, Hereditary, Leber/physiopathology; Pupil/physiology; Retinal Ganglion Cells/pathology; Retinal Ganglion Cells/physiology; Rod Opsins/physiology; Vision Disorders/etiology; Vision, Monocular |
| Tipo |
info:eu-repo/semantics/article article |
