| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4029891 | Ophthalmology | 2006 | 9 Pages |
Abstract
This gene analysis revealed a novel PITX2 mutation and a polymorphism in a family with ARAS. Whether FED, also manifested in the severely affected individuals, is due to a different but cosegregating gene is to be determined.
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Authors
Christoph MD, Malgorzata Lic Phil, Michael A. MD, PhD, Joerg MD, Alessandra PhD, Balder P. MD,