F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B.
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DOI: 10.1016/j.thromres.2022.03.010
Abstract: INTRODUCTION Hemophilia B (HB) is a hereditary bleeding disorder caused by the genetic variation of the coagulation factor IX (FIX) gene (F9). Several F9 structural abnormalities, including large deletion and/or insertion, have been observed to… read more here.
Keywords: mrna splicing; deep intronic; patient moderate; variation ... See more keywords