Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia

• Main Authors: Tham Thi Tran (Author), Quang Van Vu (Author), Taizo Wada (Author), Akihiro Yachie (Author), Huong Le Thi Minh (Author), Sang Ngoc Nguyen (Author)
• Format: Book
• Published: Hindawi Limited, 2018-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...