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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Hlavní autoři:	Tham Thi Tran, Quang Van Vu, Taizo Wada, Akihiro Yachie, Huong Le Thi Minh, Sang Ngoc Nguyen
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wiley 2018-01-01
Edice:	Case Reports in Pediatrics
On-line přístup:	http://dx.doi.org/10.1155/2018/2798621
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