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Ophthalmic Genetics, Vol. 33, Iss. 2, 2012-06 ,pp. : 119-121

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A Novel PAX6 Mutation in Chinese Patients with Severe Congenital Aniridia

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Mutation Analysis of PAX6 in a Chinese Family and a Patient with a Presumed Sporadic Case of Congenital Aniridia

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Ophthalmic Research, Vol. 47, Iss. 1, 2011-06 ,pp. : 27-31

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Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation

By Bamiou Doris-Eva   Campbell Nicole   Musiek Frank   Taylor Rachael   Chong W. K.   Moore Anthony   van Heyningen Veronica   Free Samantha   Sisodiya Sanjay   Luxon Linda  

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Novel and De-novo Truncating PAX6 Mutations and Ocular Phenotypes in Thai Aniridia Patients

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