| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4004905 | American Journal of Ophthalmology | 2007 | 4 Pages |
Abstract
A novel mutation, c.2848_2849delGA in OPA1, was identified in a Chinese family with ADOA. This mutation is associated with hearing loss, but likely not high myopia.
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Authors
Suqin PhD, Yanling MD, PhD, Yiming MD, PhD, Weili MS, Shuang MS, Xin BS, Lei Wang, Mei MD, PhD, Zuguo MD, PhD,