A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency

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Title
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency
Authors
Keywords
-
Journal
HAEMATOLOGICA
Volume -, Issue -, Pages haematol.2019.230250
Publisher
Ferrata Storti Foundation (Haematologica)
Online
2020-01-10
DOI
10.3324/haematol.2019.230250

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