Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract

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Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2018

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Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

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Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

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Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

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Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

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Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

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Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

@nl

P1476

Two Paired Box 6 mutations ide ...... ngenital aniridia and cataract

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Bingqian Liu

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Cancan Lyu

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Chenjin Jin

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Chuan Chen

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Haichun Li

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Hongbin Gao

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Lin Lu

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Qingxiu Wu

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Tao Li

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Xiaoling Liang

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P2860

Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding

The human PAX6 gene is mutated in two patients with aniridia

Induction of ectopic eyes by targeted expression of the eyeless gene in Drosophila

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

PAX6 mutations in aniridia

WAGR syndrome: a clinical review of 54 cases

The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.

LOVD v.2.0: the next generation in gene variant databases.

Bilateral sporadic aniridia: review of management.

Clinical features of Korean patients with congenital aniridia.

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scholarly article

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10.3892/MMR.2018.9469

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English

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2018-09-10T00:00:00Z

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30221735

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P932

6172400

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