Harvard Catalyst Profiles

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Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders.

Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders. Genet Couns. 2013; 24(3):253-8.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.