Next-Generation Sequencing in the Study of Platelets

Author:

Leo Vincenzo C.

Publisher

Springer International Publishing

Reference144 articles.

1. Abuzenadah AM, Zaher GF, Dallol A et al (2013) Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing. J Thromb Thrombolysis 36:501–506

2. Adler DH, Cogan JD, Phillips JA et al (2008) Inherited human cPLA 2 α deficiency is associated with impaired eicosanoid biosynthesis, small intestinal ulceration, and platelet dysfunction. J Clin Invest 118:2121–2131

3. Al Daama SA, Housawi YH, Dridi W (2013) To the editor: A missense mutation in ANKRD26 segregates with thrombocytopenia. Blood 122:461–462

4. Albers CA, Cvejic A, Favier R et al (2011) Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nat Genet 43:735–737

5. Albers CA, Paul DS, Schulze H et al (2012) Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nat Genet 44(435–9):S1–S2

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