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Short Communication

High-resolution melting analysis for detection of MYH9 mutations

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Pages 471-475 | Received 22 Nov 2007, Accepted 18 Apr 2008, Published online: 07 Jul 2009

References

  • Simons M, Wang M, McBride OW, Kawamoto S, Yamakawa K, Gdula D, Adelstein RS, Weir L. Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes. Circ Res 1991; 69: 530–539
  • Heath KE, Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, et al. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes. Am J Hum Genet 2001; 69: 1033–1045
  • Hegglin R. Gleichzeitige konstitutionelle veranderungen an Neutrophilen und thrombocyten. Helv Med Acta 1945; 12: 439–440
  • May R. Leukozyteneinschlusse. Deut Arch Klin Med 1909; 96: 1–6
  • Mhawech P, Saleem A. Inherited giant platelet disorders. Classification and literature review. Am J Clin Pathol 2000; 113: 176–190
  • Seri M, Cusano R, Gangarossa S, Caridi G, Bordo D, Lo Nigro C, Ghiggeri GM, Ravazzolo R, Savino M, Del Vecchio M, et al. Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes, May-Hegglin/Fechtner Syndrome Consortium. Nat Genet 2000; 26: 103–105
  • Kelley MJ, Jawien W, Ortel TL, Korczak JF. Mutation of MYH9, encoding non-muscle myosin heavy chain, in May-Hegglin anomaly. Nat Genet 2000; 26: 108–110

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