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25. Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report. Park J, Yhim HY, Kang KP, Bae TW, Cho YG. Hematology; 2022 Dec 01; 27(1):603-608. PubMed ID: 35617302 [Abstract] [Full Text] [Related]
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