Mutations in the nonmuscle myosin heavy chain IIA gene (MYH9) result in the diverse phenotypes of the May-Hegglin anomaly, Fechtner and Sebastian syndromes.
Abstract
Publication Date:
2000
Iris type:
1.5 Abstract in rivista
Keywords:
nonmuscle myosin heavy chain IIA gene; MYH9; Inherited thrombocytopeni
List of contributors:
Heath, K. E.; Seri, M.; Savino, M.; Cusano, R.; Gangarossa, S.; Caridi, G.; Bordo, D.; Lo Nigro, C.; Ghiggeri, G. M.; Del Vecchi, M.; D'Apolito, M.; Iolascon, A.; Bordo, S.; Zelante, L. L.; Balduini, Carlo; Noris, Patrizia; Magrini, Umberto; Belletti, S.; Babcock, M.; Aliprandis, E.; Glucksman, M. J.; Bizzaro, N.; Desnick, R. J.; Ravazzolo, R.; Savoia, A.; Martignetti, J. A.
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