Fazel, A <br/><br/>
Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity.  [electronic resource] 

 -  Allergologia et immunopathologia   
 - 82-86 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1578-1267 
<br/><br/><label>Standard No.: </label>10.1016/j.aller.2016.08.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Cortex Hormones--therapeutic use<br/>Autoimmunity--genetics<br/>Child<br/>Cytidine Deaminase--genetics<br/>DNA Mutational Analysis<br/>Dwarfism, Pituitary--genetics<br/>Female<br/>Genotype<br/>Growth Hormone--therapeutic use<br/>Hormone Replacement Therapy<br/>Humans<br/>Hyper-IgM Immunodeficiency Syndrome--genetics<br/>Immunoglobulin M--blood<br/>Infant<br/>Iran<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Phenotype<br/>AICDA (Activation-Induced Cytidine Deaminase)