| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4004880 | American Journal of Ophthalmology | 2007 | 8 Pages |
Abstract
The OPA1 IVS 8 +32 T/C polymorphism is associated with NTG, and may be used as a marker for this disease association. This polymorphism also influences the phenotypic feature in patients with HTG and should be considered to be a genetic risk factor not only for NTG, but also for HTG.
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Authors
Fumihiko MD, PhD, Sa MD, PhD, Kenji MD, PhD, Zentaro MD, PhD, Hiroyuki MD, PhD, Shigeo MD, PhD,