An extremely rare splice site mutation in the gene encoding...

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Journal of Clinical Apheresis 2017 / 04

An extremely rare splice site mutation in the gene encoding complement factor I in a patient with atypical hemolytic uremic syndrome

Ipe, Tina S., Lim, Jooeun, Reyes, Meredith Anne, Ero, Mike, Leveque, Christopher, Lewis, Bradley, Kain, Jamey
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Language:
english
Journal:
Journal of Clinical Apheresis
DOI:
10.1002/jca.21549
Date:
April, 2017
File:
PDF, 591 KB
english, 2017
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