Mutation Analysis of PAX6 in a Chinese Family and a Patient with a Presumed Sporadic Case of Congenital Aniridia | Citedby Results | Ophthalmic Research | Karger Publishers

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

Ophthalmic Res (2011) 47 (1): 27–31.

This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.

PAX6 allelic heterogeneity in Mexican congenital aniridia patients: expanding the mutational spectrum with seven novel pathogenic variants

Sofía Pérez‐Solórzano
Oscar F Chacón‐Camacho
Mirena C Astiazarán
Gerardo Ledesma‐Gil
Juan Carlos Zenteno

Clinical & Experimental Ophthalmology (2017) 45 (9): 875.