Multiethnic involvement in autosomal-dominant optic atrophy in Singapore

PURPOSE: Autosomal-dominant optic atrophy (ADOA), often associated with mutations in the OPA1 gene (chromosome 3q28-q29) is rarely reported in Asia. Our aim was to identify and describe this condition in an Asian population in Singapore. PATIENTS AND METHODS: Preliminary cross-sectional study at the...

詳細記述

保存先:
書誌詳細
出版年:Eye (Lond)
主要な著者: Loo, J L, Singhal, S, Rukmini, A V, Tow, S, Amati-Bonneau, P, Procaccio, V, Bonneau, D, Gooley, J J, Reynier, P, Ferré, M, Milea, D
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group 2017
主題:
Clinical Study
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5350376/
https://ncbi.nlm.nih.gov/pubmed/27858935
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/eye.2016.255
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