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A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly

✍ Scribed by Doucette, Lance; Green, Jane; Fernandez, Bridget; Johnson, Gordon J; Parfrey, Patrick; Young, Terry-Lynn


Book ID
109849319
Publisher
Nature Publishing Group
Year
2010
Tongue
English
Weight
452 KB
Volume
19
Category
Article
ISSN
1018-4813

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