Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia (Q24317727)

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Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia
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    Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia (English)
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    Michael Kirwan
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    Amanda J Walne
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    Inderjeet Dokal
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    4 May 2012
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    90
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    888-92
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    5
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