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[The mutation IVS2 -2A-- > C of SEDL gene was firstly determined in the world/change of the splice acceptor in SEDL intron 2 may cause skipping of exon 3 which is responsible for the X-linked spondyloepiphyseal dysplasia tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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