Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

@en

Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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P1476

Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

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P2093

Bo-Wen Zhang

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Fei-Fei Cheng

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Huan-Yun Yu

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Kai-Wen He

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Lue Xiang

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Ru-Yi Han

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Si-Si Zheng

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Wan Cheng

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Wenjuan Zhuang

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Xiao-Tao Xu

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Paired-type homeodomain transcription factors are imported into the nucleus by karyopherin 13

Regulation of microphthalmia-associated transcription factor MITF protein levels by association with the ubiquitin-conjugating enzyme hUBC9

P2888

s12276-018-0079-0

P304

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P31

scholarly article

P356

10.1038/S12276-018-0079-0

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P433

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P478

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P577

2018-04-27T00:00:00Z

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P698

29700284

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P932

5938035

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