Heterozygous FOXC1 Mutation (M161K) Associated with Congenital Glaucoma and Aniridia in an Infant and a Milder Phenotype in Her Mother

Author: Khan Arif   Aldahmesh Mohammad   Al-Amri Abdullah  

Publisher: Informa Healthcare

ISSN: 1381-6810

Source: Ophthalmic Genetics, Vol.29, Iss.2, 2008-06, pp. : 67-71

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