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- W1991644290 abstract "CEP152 is a genome maintenance protein disrupted in Seckel syndrome Kalay et al. (2011) Nature Genetics 43(1):23–26" @default.
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- W1991644290 date "2011-03-13" @default.
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- W1991644290 title "Step to CEP152: uncovering a new mutation implicated in Seckel syndrome" @default.
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- W1991644290 doi "https://doi.org/10.1111/j.1399-0004.2011.01655.x" @default.
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