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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Detalles Bibliográficos
Autores principales: Tran, Tham Thi, Vu, Quang Van, Wada, Taizo, Yachie, Akihiro, Le Thi Minh, Huong, Nguyen, Sang Ngoc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288574/
https://www.ncbi.nlm.nih.gov/pubmed/30598852
http://dx.doi.org/10.1155/2018/2798621

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288574/
https://www.ncbi.nlm.nih.gov/pubmed/30598852
http://dx.doi.org/10.1155/2018/2798621

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