The many causes of severe congenital neutropenia
- PMID: 19118300
- PMCID: PMC4162527
- DOI: 10.1056/NEJMp0806821
The many causes of severe congenital neutropenia
Comment on
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A syndrome with congenital neutropenia and mutations in G6PC3.N Engl J Med. 2009 Jan 1;360(1):32-43. doi: 10.1056/NEJMoa0805051. N Engl J Med. 2009. PMID: 19118303 Free PMC article.
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References
-
- Klein C, Grudzien M, Appaswamy G, et al. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet. 2007;39:86–92. - PubMed
-
- Dale DC, Person RE, Bolyard AA, et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood. 2000;96:2317–22. - PubMed
-
- Köllner I, Sodeik B, Schreek S, et al. Mutations in neutrophil elastase causing congenital neutropenia lead to cytoplasmic protein accumulation and induction of the unfolded protein response. Blood. 2006;108:493–500. - PubMed
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