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ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism.
Faleschini, Michela; Ammeti, Daniele; Papa, Nicole; Alfano, Caterina; Bottega, Roberta; Fontana, Giorgia; Capaci, Valeria; Zanchetta, Melania E; Pozzani, Federico; Montanari, Francesca; Petroni, Valeria; Giordano, Paola; Noris, Patrizia; Giona, Fiorina; Savoia, Anna.
Afiliação
  • Faleschini M; Istitute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste.
  • Ammeti D; Istitute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste.
  • Papa N; Department of Medical Sciences, University of Trieste, Trieste.
  • Alfano C; Structural Biology and Biophysics Unit, Fondazione Ri.MED, Palermo.
  • Bottega R; Istitute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste.
  • Fontana G; Istitute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste.
  • Capaci V; Department of Medical Sciences, University of Trieste, Trieste.
  • Zanchetta ME; Istitute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste.
  • Pozzani F; Department of Life Sciences, University of Trieste, Trieste.
  • Montanari F; Sant'Orsola-Malpighi University Hospital, Medical Genetics Unit, Bologna.
  • Petroni V; SOSD Pediatric Oncohematology, University Hospital "Ospedali Riuniti", Ancona.
  • Giordano P; Interdisciplinary department of Medicine, Pediatric Unit, University "A.Moro" of Bari, Bari.
  • Noris P; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation, University of Pavia, Pavia.
  • Giona F; Department of Translational and Precision Medicine, Sapienza University of Rome, Rome.
  • Savoia A; Istitute for Maternal and Child Health - IRCCS Burlo Garofolo, Trieste, Italy; Department of Medical Sciences, University of Trieste, Trieste. anna.savoia@burlo.trieste.it.
Haematologica ; 107(9): 2249-2254, 2022 09 01.
Article em En | MEDLINE | ID: mdl-35586967
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article