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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Bibliografische gegevens
Gepubliceerd in:Case Rep Pediatr
Hoofdauteurs: Tran, Tham Thi, Vu, Quang Van, Wada, Taizo, Yachie, Akihiro, Le Thi Minh, Huong, Nguyen, Sang Ngoc
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi 2018
Onderwerpen:
Research Article
Online toegang: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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