Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in The Absence Of Molecular Diagnosis
Author:
Affiliation:
1. National Institute of Immunohaematology-ICMR; Mumbai India
Funder
Foundation of Primary Immunodeficiency (FPID)
Publisher
Wiley
Subject
Immunology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/sji.12621/fullpdf
Reference12 articles.
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2. A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity;Matute;Blood,2009
3. Genetic and biochemical background of chronic granulomatous disease;Jurkowska;Arch Immunol Ther Exp (Warsz),2004
4. Genetic, biochemical, and clinical features of chronic granulomatous disease;Segal;Medicine,2000
5. Chronic granulomatous disease: two decades of experience from a tertiary care centre in North West India;Rawat;J Clin Immunol,2014
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