(Q24624430)

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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration (English)
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Irma Lopez
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Huanan Ren
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Yiyun Chen
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Yumei Li
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Gerald A Fishman
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Mohammed Genead
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Naimesh Solanki
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Elias I Traboulsi
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Jingliang Cheng
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Martin McKibbin
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Bruce E Hayward
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Colin A Johnson
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Mohammed Nageeb
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Moin D Mohamed
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Hussain Jafri
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Yasmin Rashid
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Graham R Taylor
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Vafa Keser
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Graeme Mardon
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Huidan Xu
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Qing Fu
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Rui Chen
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September 2012
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44
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9
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1035-9
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