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[Our results suggest that the 20% to 50% of missingCOL4A5 mutations in X-linked Alport syndrome may be rearrangements similar to that reported here, which was not detectable by sequencing of either individual COL4A5 exons or overlapping cDNA fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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