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

Publisher： Karger

E-ISSN： 1423-0259|47|1|27-31

ISSN： 0030-3747

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

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