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Case Reports in Pediatrics
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Case Reports in Pediatrics
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2018
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Article
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Fig 3
/
Research Article
Novel
HAX1
Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
Figure 3
A novel homozygous frameshift mutation (c.423_424insG, p.Gly143fs) found in the
HAX1
gene (exon 3).
(a)
(b)