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- W2040257146 abstract "Abstract: We present an infant with AEC syndrome due to a novel TP63 mutation (F552S), who demonstrated neonatal erythroderma followed by extensive depigmentation. We are unaware of previous reports highlighting the extensive depigmentation present in our patient." @default.
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- W2040257146 date "2009-09-01" @default.
- W2040257146 modified "2023-10-15" @default.
- W2040257146 title "AEC Syndrome Caused by a Novel p63 Mutation and Demonstrating Erythroderma Followed by Extensive Depigmentation" @default.
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- W2040257146 doi "https://doi.org/10.1111/j.1525-1470.2009.00997.x" @default.
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