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Novel and Recurrent Mutations in the C1NH Gene of Arab Patients Affected with Hereditary Angioedema
International Archives of Allergy and Immunology, 09/17/09
Faiyaz–Ul–Haque M et al. – This is the first ever report of C1NH gene mutations in Middle Eastern Arab patients. The study suggests that, despite the numerous existing mutations in the C1NH gene, there are novel and recurrent mutations in HAE patients of non–European origin. It is concluded that the spectrum of C1NH gene mutations in HAE patients is wider due to the likely presence of novel and recurrent mutations in patients of other ethnicities.
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