MYH9 gene mutations associated with bleeding
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DOI: 10.1080/09537104.2017.1294250
Abstract: MYH9 is a large gene localized on chromosome 22q12.3-13.1 constituted of one 5ˊ-untranslated (exon 1) and 40 coding exons (Figure 1). It encodes for the heavy chain of the nonmuscle myosin IIA (NMMHC-IIA), a cytoplasmic… read more here.
Keywords: thrombocytopenia; myh9; nmmhc iia; nonhelical tail ... See more keywords