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Sep 2013;30(9):1147-56

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DNA sequencing identified two putative null mutants, Gmmorf2a/b-1 and Gmmorf2a/b-2 , which harbored non multiple of 3-bp deletions in the first exon of GmMORF2a and GmMORF2b , causing frameshifts and premature termination of protein translation (Supplementary Fig

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