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Paper Details

A novel homozygous VPS45 p.P468L mutation leading to severe congenital neutropenia with myelofibrosis.
Pediatr Blood Cancer
12
2017
SCN, SNARE, VPS45, VPS45 "hinge" region, congenital neutropenia, filgrastim, myelofibrosis, neutropenia, neutrophil and platelet dysfunction, patient, rare, stem cell
Author NameAffiliation
Mary MunsonUniversity of Massachusetts Medical School
Peter E NewburgerUniversity of Massachusetts Medical School
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Release 1.2