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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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| Publicado no: | Case Rep Pediatr |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6288574/ https://ncbi.nlm.nih.gov/pubmed/30598852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/2798621 |
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