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Mutations of a Human Homologue of the Drosophila Eyes Absent Gene (EYA1) Detected in Patients With Congenital Cataracts and Ocular Anterior Segment Anomalies
Human Molecular Genetics
- United Kingdom
doi 10.1093/hmg/9.3.363
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Categories
Medicine
Genetics
Molecular Biology
Date
February 12, 2000
Authors
N. Azuma
Publisher
Oxford University Press (OUP)
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