A novel homozygous VPS45 p.P468L mutation leading to severe congenital neutropenia with myelofibrosis
Shah, Rikin K., Munson, Mary, Wierenga, Klaas J., Pokala, Hanumantha R., Newburger, Peter E., Crawford, DavidLanguage:
english
Journal:
Pediatric Blood & Cancer
DOI:
10.1002/pbc.26571
Date:
April, 2017
File:
PDF, 467 KB
english, 2017