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pro vyhledávání: '"Strachan, Elin L."'
Autor:
Strachan, Elin L., Mac White-Begg, Delphi, Crean, John, Reynolds, Alison, Kennedy, Breandán, O'Sullivan, Niamh C.
Optic atrophy (OA) with autosomal inheritance is a form of optic neuropathy characterized by the progressive and irreversible loss of vision. In some cases, this is accompanied by additional, typically neurological, extra-ocular symptoms. Underlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1061::de89fffd19166a68399651e9f81ad780
Autor:
Strachan EL; UCD Conway Institute, University College Dublin, Dublin, Ireland.; UCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland., Mac White-Begg D; UCD Conway Institute, University College Dublin, Dublin, Ireland.; UCD School of Veterinary Medicine, University College Dublin, Dublin, Ireland., Crean J; UCD Conway Institute, University College Dublin, Dublin, Ireland.; UCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland.; UCD Diabetes Complications Research Centre, Conway Institute of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland., Reynolds AL; UCD Conway Institute, University College Dublin, Dublin, Ireland.; UCD School of Veterinary Medicine, University College Dublin, Dublin, Ireland., Kennedy BN; UCD Conway Institute, University College Dublin, Dublin, Ireland.; UCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland., O'Sullivan NC; UCD Conway Institute, University College Dublin, Dublin, Ireland.; UCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland.
Publikováno v:
Frontiers in neuroscience [Front Neurosci] 2021 Nov 15; Vol. 15, pp. 784987. Date of Electronic Publication: 2021 Nov 15 (Print Publication: 2021).