Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
Severe congenital neutropenia (SCN) is a rare disease that involves a heterogeneous group of hereditary diseases. Mutations in the HAX1 gene can cause an autosomal recessive form of SCN-characterized low blood neutrophil count from birth, increased susceptibility to recurrent and life-threatening in...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Hindawi Limited,
2018-01-01T00:00:00Z.
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