Heterozygous FOXC1 mutation (M161K) associated with congenital glaucoma and aniridia in an infant and a milder phenotype in her mother. (Q54532643)
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scientific article published in June 2008
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English | Heterozygous FOXC1 mutation (M161K) associated with congenital glaucoma and aniridia in an infant and a milder phenotype in her mother. |
scientific article published in June 2008 |
Statements
Heterozygous FOXC1 mutation (M161K) associated with congenital glaucoma and aniridia in an infant and a milder phenotype in her mother. (English)
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Arif O Khan
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Abdullah Al-Amri
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1 June 2008
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29
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2
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67-71
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Identifiers
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