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Insights into the genetics of severe congenital neutropenia
Author(s) -
Stein RA
Publication year - 2007
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2007.00872.x
Subject(s) - congenital neutropenia , neutropenia , genetics , medicine , disease , cyclic neutropenia , biology , pathology , chemotherapy
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
Klein et al. (2007)
Nature Genetics 39: 86–92