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Mutations of RUNX1 in families with inherited thrombocytopenia.
De Rocco, Daniela; Melazzini, Federica; Marconi, Caterina; Pecci, Alessandro; Bottega, Roberta; Gnan, Chiara; Palombo, Flavia; Giordano, Paola; Coccioli, Maria Susanna; Glembotsky, Ana C; Heller, Paula G; Seri, Marco; Savoia, Anna; Noris, Patrizia.
Afiliación
  • De Rocco D; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Melazzini F; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Marconi C; Department of Medical and Surgical Science, Policlinico Sant'Orsola Malpighi and University of Bologna, Bologna, Italy.
  • Pecci A; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Bottega R; Department of Medical Sciences, University of Trieste, Trieste, Italy.
  • Gnan C; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Palombo F; Department of Medical and Surgical Science, Policlinico Sant'Orsola Malpighi and University of Bologna, Bologna, Italy.
  • Giordano P; Department of Biomedical Science and Human Oncology, Clinical Pediatrics "B. Trambusti," University of Bari, Bari, Italy.
  • Coccioli MS; U.O.C of Pediatrics, Hospital "D. Camberlingo", Francavilla Fontana, Brindisi, Italy.
  • Glembotsky AC; IDIM-CONICET, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Heller PG; IDIM-CONICET, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Seri M; Department of Medical and Surgical Science, Policlinico Sant'Orsola Malpighi and University of Bologna, Bologna, Italy.
  • Savoia A; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Noris P; Department of Medical Sciences, University of Trieste, Trieste, Italy.
Am J Hematol ; 92(6): E86-E88, 2017 06.
Article en En | MEDLINE | ID: mdl-28240786
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Mutación Missense / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Trombocitemia Esencial Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hematol Año: 2017 Tipo del documento: Article País de afiliación: Italia
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Mutación Missense / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Trombocitemia Esencial Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hematol Año: 2017 Tipo del documento: Article País de afiliación: Italia